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Hemoglobin
international journal for hemoglobin research
Volume 28, 2004 - Issue 4
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Short Communication

A New Highly Unstable α Chain Variant Causing α+‐Thalassemia: Hb Zurich Albisrieden [α59(E8)Gly→Arg (α2)]

Fabrizio Dutly Institute for Medical and Molecular Diagnostics Ltd., Rautistrasse 13, CH‐8047, Zürich, Switzerland
,
Jörg Fehr Division of Hematology, University Hospital, Zürich, Switzerland
,
Jeroen Simon Goede Division of Hematology, University Hospital, Zürich, Switzerland
,
Markus Morf Medizinische Poliklinik, University Hospital, Zürich, Switzerland
,
Heinz Troxler Department of Pediatrics, Division of Clinical Chemistry, University of Zürich, Zürich, Switzerland
&
Hannes Frischknecht Institute for Medical and Molecular Diagnostics Ltd., Rautistrasse 13, CH‐8047, Zürich, Switzerland
Pages 347-351 | Received 15 Mar 2004, Accepted 10 May 2004, Published online: 24 Aug 2009

Citations (13)

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Shao-Min Wu, Su-Ran Huang, Chan Li, Gui-Lan Chen & Dong-Zhi Li. (2022) Severe Hb H Disease Caused by Hb Zürich–Albisrieden (HBA1: c.178G>C): Another Case Report. Hemoglobin 46:6, pages 341-343.
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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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Hua Jiang, Lv-Yin Huang, Li Zhen, Fan Jiang & Dong-Zhi Li. (2017) Two α1-Globin Gene Point Mutations Causing Severe Hb H Disease. Hemoglobin 41:4-6, pages 293-296.
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Xin Yang, Jin-Mei Yan, Jian Li, Xing-Mei Xie, Jian-Ying Zhou, Yan Li & Dong-Zhi Li. (2016) Hydrops Fetalis Associated with Compound Heterozygosity for Hb Zurich-Albisrieden (HBA2: C.178G > C) and the Southeast Asian (– –SEA/) Deletion. Hemoglobin 40:5, pages 353-355.
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Jianpei Fang, Luming Chen, Ruiping Zeng, Qiuhong Tian, Weiying Jiang, Hongyi Li, Zheng Chen, Chuanshu Du & Suqin Chen. (2014) The Hb H Disease Genotypes in Southern China. Hemoglobin 38:1, pages 76-78.
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Joanne Traeger-Synodinos, Varvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, Vasilis Ladis, Tania Siahanidou, Irine Fylaktou & Emmanuel Kanavakis. (2010) Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)]. Hemoglobin 34:5, pages 430-438.
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Varvara Douna, Ioannis Papassotiriou, Anna Metaxotou-Mavrommati, Alexandra Stamoulakatou, Dimitra Liapi, Dimitrios Kampourakis, Amalia Tsilimigaki, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations. Hemoglobin 32:4, pages 379-385.
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Varvara Douna, Ioannis Papassotiriou, Anastasia Garoufi, Eleni Georgouli, Vassilis Ladis, Alexandra Stamoulakatou, Anna Metaxotou-Mavrommati, Emmanuel Kanavakis & Joanne Traeger-Synodinos. (2008) A Rare Thalassemic Syndrome Caused by Interaction of Hb Adana [α59(E8)Gly→Asp] with an α+-Thalassemia Deletion: Clinical Aspects in Two Cases. Hemoglobin 32:4, pages 361-369.
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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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Articles from other publishers (4)

Li Du, Xiuqin Bao, Wei He, Danqing Qin, Jicheng Wang, Ying Xiong, Xiaomei Shi, Hongke Ding, Cuize Yao & Jing Wu. (2021) Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden ( HBA2 :c.178G>C) and Hb Quong Sze ( HBA2 :c.377T>C) . Journal of International Medical Research 49:7, pages 030006052110314.
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Prashant Sharma, Reena Das, Alka Rani Khadwal, Indrani Karmakar, Jasbir Kaur Hira & Sanjeev Chhabra. (2020) HbH disease due to compound heterozygosity for hemoglobins Zürich‐Albisrieden and Sallanches. Pediatric Blood & Cancer 67:4.
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Gisele A. Pedroso, Elza M. Kimura, Magnun N.N. Santos, Dulcinéia M. Albuquerque, Danaê Malimpensa, Susan E. Jorge, Monica P.A. Verissimo, Fernando F. Costa & Maria F. Sonati. (2018) Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child. Pediatric Blood & Cancer 65:12, pages e27413.
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Oded Gilad, Orna Steinberg Shemer, Orly Dgany, Tanya Krasnov, Michal Nevo, Sharon Noy-Lotan, Ron Rabinowicz, Nofar Amitai, Shifra Ben-Dor, Isaac Yaniv, Joanne Yacobovich & Hannah Tamary. (2017) Molecular diagnosis of α-thalassemia in a multiethnic population. European Journal of Haematology 98:6, pages 553-562.
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