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Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 1
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Original Article

Hb Sallanches [α104(G11)Cys→Tyr]: A Rare α2-Globin Chain Variant Found in the Homozygous State in Three Members of a Pakistani Family

S. N. Khan Centre for Applied Molecular Biology, University of the Punjab Thokar Niaz Baig, Lahore, 53700, PakistanCorrespondence[email protected]
,
F. I. Butt Department of Pathology, Hematology section, Allama Iqbal Medical College, Lahore, 53700, Pakistan
,
S. Riazuddin Centre for Applied Molecular Biology, University of the Punjab Thokar Niaz Baig, Lahore, 53700, Pakistan
&
R. Galanello Istituto di Clinica e Biologia dell 'Età Evolutiva Università degli Studi di Cagliari Ospedale Regionale Microcitemie, I-09121, Cagliari, Italia
Pages 31-35 | Received 17 Aug 1999, Accepted 11 Oct 1999, Published online: 07 Jul 2009

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Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Prashant Warang, Sona Nair, Anita Nadkarni, Kanjaksha Ghosh & Roshan B. Colah. (2010) Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches. Hemoglobin 34:1, pages 45-48.
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Papai Roy, Gargi Bhattacharya, Debasish Banerjee, Sarmila Chandra, Malay Ghosh, Utpal Choudhuri, Manikanchan Das & Uma B. Dasgupta. (2009) Hb Sallanches [α104(G11)Cys→Tyr, TGC>TAC] Occurs Frequently on the Indian Subcontinent. Hemoglobin 33:6, pages 486-491.
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Henri Wajcman, Jan Traeger-Synodinos, Ioannis Papassotiriou, Piero C. Giordano, Cornelis L. Harteveld, Véronique Baudin-Creuza & John Old. (2008) Unstable and Thalassemic α Chain Hemoglobin Variants: A Cause of Hb H Disease and Thalassemia Intermedia. Hemoglobin 32:4, pages 327-349.
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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.
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Sumitra Dash, Keiko Harano & Santosh Menon. (2006) Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child. Hemoglobin 30:3, pages 393-396.
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Cornelis L. Harteveld, Lieke Rozendaal, Nico A. Blom, Shirley Lo-A-Njoe, Nicole Akkerman, Sandra Arkestijn, Peter Van Delft & Piero C. Giordano. (2005) Hb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype. Hemoglobin 29:3, pages 165-169.
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J. S. Waye, L. Walker, D. H. K. Chui, J. Lafferty & M. Kirby. (2000) Homozygous HB Sallanches [α104(G11)CYS→TYR] in a Pakistani Child with HB H Disease. Hemoglobin 24:4, pages 355-357.
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Articles from other publishers (11)

Samina Ejaz, Iqra Abdullah, Muhammad Usman, Muhammad Arslan Iqbal, Sidra Munawar, Muhammad Irfan Khan, Nagina Imtiaz, Hanniah Tahir, Muhammad Ihsan Bari, Tayyaba Rasool, Aneeza Fatima, Ramsha Anwar, Ayman Durrani & Yasir Hameed. (2023) Mutational analysis of hemoglobin genes and functional characterization of detected variants, through in-silico analysis, in Pakistani beta-thalassemia major patients. Scientific Reports 13:1.
Crossref
Samaneh Farashi & Hossein Najmabadi. (2015) Diagnostic pitfalls of less well recognized HbH disease. Blood Cells, Molecules, and Diseases 55:4, pages 387-395.
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Bushra Moiz, Mashhooda Rasool Hashmi, Amna Nasir, Anila Rashid & Tariq Moatter. (2012) Hemoglobin E syndromes in Pakistani population. BMC Blood Disorders 12:1.
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Corinne Vasseur, Elisa Domingues-Hamdi, Thomas Brillet, Michael C. Marden & Véronique Baudin-Creuza. (2009) The α-hemoglobin stabilizing protein and expression of unstable α-Hb variants. Clinical Biochemistry 42:18, pages 1818-1823.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 266 295 .
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 .
Helene Puehringer, Hossein Najmabadi, Hai-Yang Law, Walter Krugluger, Vip Viprakasit, Serge Pissard, Erol Baysal, Ali Taher, Chantal Farra, Amein Al-Ali, Suad Al-Ateeq & Christian Oberkanins. (2007) Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions. Clinical Chemical Laboratory Medicine 45:5.
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Corinne Vasseur-Godbillon, Michael C. Marden, Piero Giordano, Henri Wajcman & Véronique Baudin-Creuza. (2006) Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome. Blood Cells, Molecules, and Diseases 37:3, pages 173-179.
Crossref
John Old. 2004. Genetic Disorders of the Indian Subcontinent. Genetic Disorders of the Indian Subcontinent 245 264 .
David H. K. ChuiSuthat FucharoenVivian Chan. (2003) Hemoglobin H disease: not necessarily a benign disorder. Blood 101:3, pages 791-800.
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