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Hemoglobin
international journal for hemoglobin research
Volume 21, 1997 - Issue 5
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Original Article

Novel Mutation of the α2-Globin Gene Initiation Codon (Atg→A-G) in a Vietnamese Girl with Hb H Disease

J. S. Waye Provincial Hemoglobinopathy DNA Diagnostic, Laboratory McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
B. Eng Provincial Hemoglobinopathy DNA Diagnostic, Laboratory McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
M. Patterson Provincial Hemoglobinopathy DNA Diagnostic, Laboratory McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
D. H.K. Chui Provincial Hemoglobinopathy DNA Diagnostic, Laboratory McMaster University Medical Centre Hamilton, Ontario, L8N 3Z5, Canada
,
E. Nisbet-Brown The Hospital for Sick Children Toronto, Ontario, M5G 1X8, Canada
&
N. F. Olivieri The Hospital for Sick Children Toronto, Ontario, M5G 1X8, Canada
Pages 469-472 | Received 02 Apr 1997, Accepted 30 Jun 1997, Published online: 07 Jul 2009

Citations (8)

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Read on this site (4)

John S. Waye, Barry Eng, Meredith Hanna, Betty-Ann Hohenadel, Lisa Nakamura & Lynda Walker. (2016) Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A). Hemoglobin 40:5, pages 369-370.
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Barry Eng, Margie Patterson, Lynda Walker, Carolyn Hoppe, Mahin Azimi, Helen Lee, Piero C. Giordano & John S. Waye. (2006) Three New α-Thalassemia Point Mutations Ascertained Through Newborn Screening. Hemoglobin 30:2, pages 149-153.
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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.
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T. H.J. Huisman & M. F.H. Carver. (1998) The Thalassemia Repository (Ninth Edition; Part II). Hemoglobin 22:3, pages 287-310.
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Articles from other publishers (4)

Félix de la Fuente-Gonzalo, Jorge M. Nieto, Diego Velasco, Elena Cela, Germán Pérez, Ana Fernández-Teijeiro, Antonio Escudero, Ana Villegas, Fernando A. González-Fernández & Paloma Ropero. (2016) HB Puerta del Sol [HBA1:c.148A>C], HB Valdecilla [HBA2:c.3G>T], HB Gran Vía [HBA2:c.98T>G], HB Macarena [HBA2:c.358C>T] and HB El Retiro [HBA2:c.364_366dupGTG]: description of five new hemoglobinopathies. Clinical Chemistry and Laboratory Medicine (CCLM) 54:4.
Crossref
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallDouglas R. Higgs. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin 239 240 .
John S. Waye, Barry Eng, Margaret Patterson, Lynda Walker, Manuel D. Carcao, Nancy F. Olivieri & David H.K. Chui. (2001) Hemoglobin H (Hb H) disease in Canada: Molecular diagnosis and review of 116 cases. American Journal of Hematology 68:1, pages 11-15.
Crossref
F. KUTLAR, T. V. ADAMKIEWICZ, R. B. MARKOWITZ, L. HOLLEY & A. KUTLAR. (1998) An alpha-2 Globin Gene Initiation Codon Mutation in a Vietnamese Patient with Hb H Disease. Annals of the New York Academy of Sciences 850:1 COOLEY'S ANEM, pages 398-400.
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