Advanced search
Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 3, 1979 - Issue 2-3
Submit an article Journal homepage
23
Views
53
CrossRef citations to date
0
Altmetric
Original Article

Hemoglobin Suan-Dok (α2109(G16)LEU-ARGβ2). an Unstable Variant Associated with α-Thalassemia

T. Sanguansermsri Department of Pediatrics and Human Genetics Unit, Faculty of Medicine, Chiangmai University, Chiangmai, Thailand
,
S. Matragoon Department of Pediatrics and Human Genetics Unit, Faculty of Medicine, Chiangmai University, Chiangmai, Thailand
,
L. Changloah Department of Pediatrics and Human Genetics Unit, Faculty of Medicine, Chiangmai University, Chiangmai, Thailand
&
G. Flatz Institut für Genetik, Medizinische Hochschule Hannover, Hannover, Federal Republick of Germany
Pages 161-174 | Received 13 Oct 1978, Accepted 21 Feb 1979, Published online: 07 Jul 2009

Citations (53)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (32)

Sitthichai Panyasai, Kanyakan Kongthai & Amphai Phasit. (2020) Association of Hb Shenyang [α26(B7)Ala→Glu, GCG>GAG, HBA2: c.80C>A (or HBA1)] with Several Types of α-Thalassemia in Thailand. Hemoglobin 44:5, pages 354-360.
Read now
Cristina Curcio, Valentina Giannone, Elena Benzoni, Claudia Cesaretti & Giovanni Ivaldi. (2019) Hb Milano [α109(G16)Leu→Pro (CTG>CCG); HBA1: c.329T>C]: A Novel Variant on the α1-Globin Gene in an Italian Family. Hemoglobin 43:1, pages 4-6.
Read now
Samaneh Farashi, Negin Faramarzi Garous, Mehri Ashki, Shadi Vakili, Fatemah Zeinali, Hashem Imanian, Azita Azarkeivan & Hossein Najmabadi. (2015) Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient. Hemoglobin 39:3, pages 152-155.
Read now
Kamran Moradkhani, Elodie Mazurier, Piero C. Giordano, Henri Wajcman & Claude Préhu. (2008) An α0-Thalassemia-Like Mutation: Hb Suan-Dok [α109(G16)Leu→Arg] Carried by a Recombinant −α3.7 Gene. Hemoglobin 32:4, pages 419-424.
Read now
Cornelis L. Harteveld, Florens G.A. Versteegh, Peter J.M.J. Kok, Irene H. van Rooijen-Nijdam, Peter van Delft & Piero C. Giordano. (2006) Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: A New Abnormal Hemoglobin Associated with a Mild α-Thalassemia Phenotype. Hemoglobin 30:3, pages 349-354.
Read now
Vip Viprakasit, Worrawut Chinchang, Waraporn Glomglao & Voravarn S Tanphaichitr. (2005) A Rare Association of α0-Thalassemia (– –SEA) and an Initiation Codon Mutation (ATG→A-G) of the α2 Gene Causes Hb H Disease in Thailand. Hemoglobin 29:3, pages 235-240.
Read now
Marlies E. Regtuijt, Cornelis L. Harteveld, Peter Van Delft, Nicole Akkermans & Piero C. Giordano. (2004) Hb Suan‐Dok [α109(G16)Leu→Arg; CTG→CGG (α2)] Described in a Patient of African Ancestry. Hemoglobin 28:3, pages 173-176.
Read now
T. H.J. Huisman & M. F.H. Carver. (1998) The Thalassemia Repository (Ninth Edition; Part II). Hemoglobin 22:3, pages 287-310.
Read now
Suthat Fucharoen & Pranee Winichagoon. (1997) Hemoglobinopathies in Southeast Asia: Molecular Biology and Clinical Medicine. Hemoglobin 21:4, pages 299-319.
Read now
M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
Read now
. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
Read now
. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
Read now
. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
Read now
. (1992) Variants of the Alpha Chain. Hemoglobin 16:3, pages 127-213.
Read now
. (1991) International hemoglobin information center: Variants of the alpha chain. Hemoglobin 15:3, pages 139-217.
Read now
Y. Ohba. (1990) Unstable Hemoglobins. Hemoglobin 14:4, pages 353-388.
Read now
. (1990) International Hemoglobin Information Center. Hemoglobin 14:3, pages 249-325.
Read now
J. Hundrieser, T. Sanguansermsri, M. Laig, M. Pape, W. Kiihnau & G. Flatz. (1990) Direct Demonstration of the hb Suan-Dok Mutation in the Q2-Globin Gene by Restriction Analysis with Sma I. Hemoglobin 14:1, pages 69-77.
Read now
. (1989) Variants of the Alpha Chain. Hemoglobin 13:3, pages 223-297.
Read now
. (1988) IHIC Variants List. Hemoglobin 12:3, pages 209-282.
Read now
P. Yinichagoon, V. Thonglairuam, S. Fucharoen, V. S. Tanphaichito & P. Wasi. (1988) α-Thaiassemia in Thailand. Hemoglobin 12:5-6, pages 485-498.
Read now
S. Fucharoen & P. Winichagoon. (1987) Hemoglobinopathies in Southeast Asia. Hemoglobin 11:1, pages 65-88.
Read now
Y. Ohba, K. Yamaoto, Y. Hattori, R. Kawata & T. Miyaji. (1987) Hyperunstable Hemoglobin Toyama [α2136(H19)LEU→ARGβ2]: Detection and Identification by in Vitro Biosynthesis with Radioactive Amino Acids. Hemoglobin 11:6, pages 539-556.
Read now
. (1987) IHIC Variants List. Hemoglobin 11:3, pages 243-308.
Read now
. (1986) International Hemoglobin Information Center IHIC Variants List. Hemoglobin 10:3, pages 261-327.
Read now
. (1985) International Hemoglobin Information Center. Hemoglobin 9:3, pages 229-298.
Read now
. (1984) International Hemoglobin Information Center: Variants of the Alpha Chain. Hemoglobin 8:3, pages 243-300.
Read now
. (1983) International Hemoglobin Information Center: Policies—Ihic. Hemoglobin 7:4, pages 331-406.
Read now
. (1982) International Hemoglobin Information Center Policies - IHIC. Hemoglobin 6:3, pages 257-346.
Read now
. (1981) International Hemoglobin Information Center Policies - Ihic. Hemoglobin 5:3, pages 259-323.
Read now
. (1979) International Hemoglobin Information Center: Policies -Ihic. Hemoglobin 3:6, pages 481-513.
Read now
. (1979) International Hemoglobin Information Center Policies - Ihic. Hemoglobin 3:5, pages 371-395.
Read now

Articles from other publishers (21)

Duantida Songdej & Suthat Fucharoen. (2022) Alpha-Thalassemia: Diversity of Clinical Phenotypes and Update on the Treatment. Thalassemia Reports 12:4, pages 157-172.
Crossref
Kesara Nittayaboon & Chamnong Nopparatana. (2018) Molecular characterization of Hb H disease in southern Thailand. International Journal of Hematology 108:4, pages 384-389.
Crossref
Emmanuel Bissé, Christine Schaeffer-Reiss, Alain Van Dorsselaer, Tchilabalo Dilezitoko Alayi, Thomas Epting, Karl Winkler, Andres S. Benitez Cardenas, Jayashree Soman, Ivan Birukou, Premila P. Samuel & John S. Olson. (2017) Hemoglobin Kirklareli (α H58L), a New Variant Associated with Iron Deficiency and Increased CO Binding. Journal of Biological Chemistry 292:6, pages 2542-2555.
Crossref
Jin Ai Mary Anne Tan, Siew Leng Kho, Chin Fang Ngim, Kek Heng Chua, Ai Sim Goh, Seoh Leng Yeoh & Elizabeth George. (2016) DNA studies are necessary for accurate patient diagnosis in compound heterozygosity for Hb Adana (HBA2:c.179>A) with deletional or nondeletional α-thalassaemia. Scientific Reports 6:1.
Crossref
V. Viprakasit. (2015) α−thalassaemia: a genotype–phenotype correlation and management. ISBT Science Series 10:S1, pages 295-304.
Crossref
Cornelis L Harteveld & Douglas R Higgs. (2010) α-thalassaemia. Orphanet Journal of Rare Diseases 5:1.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 241 265 .
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
Viroj Wiwanitkit. (2005) Modeling for tertiary structure of globin chain in Hemoglobin Suan-Dok disorder. Hematology 10:2, pages 163-165.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Takamasa Yamaguchi, Yi Yang, Melisenda J. McDonald & Kazuhiko Adachi. (2000) Surface and Interface β-Chain Residues Synergistically Affect Hemoglobin Assembly. Biochemical and Biophysical Research Communications 270:3, pages 683-687.
Crossref
Luigi F. Bernini & Cornelis L. Harteveld. (1998) 2 α-Thalassaemia. Baillière's Clinical Haematology 11:1, pages 53-90.
Crossref
F. Morlé, A. Francina, R. Ducrocq, H. Wajcman, C. Gonnet, N. Philippe, G. Souillet & J. Godet. (2008) A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with HbH disease in one homozygous patient. British Journal of Haematology 91:3, pages 608-611.
Crossref
T. P. Molchanova, D. D. Pobedimskaya & T. H. J. Huisman. (1994) The differences in quantities of α2-and α1-globin gene variants in heterozygotes. British Journal of Haematology 88:2, pages 300-306.
Crossref
Georgina W. Hall, Swee Lay Thein, Adrian C. Newland, Morag Chisholm, Jan Traeger‐Synodinos, E. Kanavakis, C. Kattamis & Douglas R. Higgs. (2008) A base substitution (T→C) in codon 29 of the α2‐globin gene causes α thalassaemia. British Journal of Haematology 85:3, pages 546-552.
Crossref
Douglas R. Higgs. (1993) 5 α-Thalassaemia. Baillière's Clinical Haematology 6:1, pages 117-150.
Crossref
Martin H. Steinberg. (1991) The Interactions of α -Thalassemia with Hemoglobinopathies. Hematology/Oncology Clinics of North America 5:3, pages 453-473.
Crossref
VIRGIL F. FAIRBANKS, RICHARD T. JONES, CHARLOTTE HEAD, STEVEN R. VOGEL, RHAIZA OLIVEROS, BERNADINE BRIMHALL, MURRAY N. SILVERSTEIN & RAINIS BERZINS. (1990) Two Families With Hemoglobin Sogn, β(A11)14 Leu→Arg, in Minnesota and Indiana: Hematologic, Functional, and Biosynthetic Features. Mayo Clinic Proceedings 65:6, pages 793-798.
Crossref
Martin H. Steinberg. (1988) Review: Thalassemia: Molecular Pathology and Management. The American Journal of the Medical Sciences 296:5, pages 308-321.
Crossref
S. Safaya, P. Mullaney & R. F. Rieder. (1987) Dysfunctional α-globin genes in hemoglobin H disease in blacks: Variation in restriction fragment size permits the detection of the -α/-αT genotype. American Journal of Hematology 26:4, pages 329-339.
Crossref
YUET KAN. (1985) Molecular Pathology of ?-Thalassemia. Annals of the New York Academy of Sciences 445:1 Fifth Cooley', pages 28-36.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.