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Hemoglobin
international journal for hemoglobin research
Volume 15, 1991 - Issue 4
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Original Article

A New β-Thalassemia Mutation (Initiation Codon ATG→GTG) Found in the Japanese Population

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Pages 317-325 | Received 05 Nov 1990, Accepted 25 Apr 1991, Published online: 07 Jul 2009

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Read on this site (12)

Raj Muhammad, Muhammad Shakeel, Shoaib U. Rehman & Muhammad A. Lodhi. (2017) Population-Based Genetic Study of β-Thalassemia Mutations in Mardan Division, Khyber Pakhtunkhwa Province, Pakistan. Hemoglobin 41:2, pages 104-109.
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Philippe Lacan, Martine Aubry, Nicole Couprie & Alain Francina. (2005) A Mutation of the β-Globin Gene Initiation Codon, ATG→AAG, Found in a French Caucasian Man. Hemoglobin 29:3, pages 225-228.
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Irénée Kueviakoe, Nathalie Gerard, Rajagopal Krishnamoorthy, Sabrina Pereira, Jacques Elion & Rolande Ducrocq. (2004) A New High A2‐β‐Thalassemia Due to a 468 bp Deletion (− 475 to − 8) in the β‐Globin Gene Promoter of the Intact β‐Globin Structural Gene. Hemoglobin 28:1, pages 69-72.
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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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Y. Ohba, Y. Hattori, T. Harano, K. Harano, Y. Fukumaki & H. Ldeguchi. (1997) β-Thalassemia Mutations in Japanese and Koreans. Hemoglobin 21:2, pages 191-200.
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E. Baysal & M. F. H. Carver. (1995) The β- and δ-Thalassemia Repository (Eighth Edition). Hemoglobin 19:3-4, pages 213-236.
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David N. Cooper. (1993) Human Gene Mutations Affecting RNA Processing and Translation. Annals of Medicine 25:1, pages 11-17.
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S. Rahbar & G. Nozari. (1993) A Novel Initiation Codon Mutation (ATG→ATT) in a β-Thalassemia Patient. Hemoglobin 17:6, pages 557-562.
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C. Wildmann, Y. Larondelle, J. L. Vaerman, R. Eeckels, P. Martiat & M. Philippel. (1993) An Initiation Codon Mutation as a Cause of β-Thalassemia in a Belgian Family. Hemoglobin 17:1, pages 19-30.
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T. H. J. Huisman. (1993) The β- and δ-Thalassemia Repository (Seventh Edition). Hemoglobin 17:5, pages 479-499.
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M. S. Koo, S. I. Kim, H. I. Cho, Y. Hattori, Y. Yamashiro, M. Hoshitani, Y. Ohba, T. Miyaji, Ku. Yamamoto & Ki. Yamamoto. (1992) A β-Thalassemia Mutation Found in Korea. Hemoglobin 16:4, pages 313-320.
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T. H. J. Huisman. (1992) The β- and δ-Thalassemia Repository. Hemoglobin 16:4, pages 237-258.
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Articles from other publishers (10)

V. VIPRAKASIT, W. CHINCHANG, L. SUWANTHOL & V. S. TANPHAICHITR. (2005) Common origin of a rare beta-globin initiation codon mutation (ATGAGG) in Asians. Clinical and Laboratory Haematology 27:6, pages 409-415.
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F.Javier Perea, Marı́a Teresa Magaña, José G Cobián, J.Yoaly Sánchez-López, Marı́a L Chávez, Guadalupe Zamudio, Marı́a A Esparza, Beatriz López-Guido & Bertha Ibarra. (2004) Molecular spectrum of β-thalassemia in the Mexican population. Blood Cells, Molecules, and Diseases 33:2, pages 150-152.
Crossref
D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
Swee Lay Thein. (1998) 3 β-Thalassaemia. Baillière's Clinical Haematology 11:1, pages 91-126.
Crossref
John S. Waye, Barry Eng, Margaret Patterson, Ronald D. Barr & David H. K. Chui. (1997) De novo mutation of the β-globin gene initiation codon (ATG→AAG) in a Northern European. American Journal of Hematology 56:3, pages 179-182.
Crossref
Britta Landin, Olle Rudolphi & BÖRje Ek. (2006) Initiation codon mutation (ATG → ATA) of the β‐globin gene causing β‐thalassemia in a Swedish family. American Journal of Hematology 48:3, pages 158-162.
Crossref
Seiichi Tsujino, Laurence A. Rubin, Sara Shanske & Salvatore DiMauro. (1994) An A-to-C substitution involving the translation initiation codon in a patient with myophosphorylase deficiency (McArdle's disease). Human Mutation 4:1, pages 73-75.
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B. Ringelhann, J. G. Szelenyi, M. Horanyi, M. Svobodova, V. Divoky, K. Indrak, S. Holl�n, A. Marosi, M. Laub & T. H. J. Huisman. (1993) Molecular characterization of ?-thalassemia in Hungary. Human Genetics 92:4, pages 385-387.
Crossref
G. W. Hall, R. A. Barnetson & S. L. Thein. (2008) Beta thalassaemia in the indigenous British population. British Journal of Haematology 82:3, pages 584-588.
Crossref
L. Saba, A. Meloni, R. Sardu, M. Travi, P. Primignani, M. C. Rosatelli & A. Cao. (1992) A novel β-thalassemia mutation (G→A) at the initiation codon of the β-globin gene. Human Mutation 1:5, pages 420-422.
Crossref

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