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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 4
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Original Article

Hb Charlieu [α106(G13)Leu→Pro (α1)]: A New Phenotypically Silent Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype

Philippe Joly Unité de Pathologie Moléculaire du Globule Rouge, Fédération de Biochimie et de Biologie Spécialisée, Hôpital Edouard Herriot, Hospices Civils & Université Claude Bernard-Lyon 1, Lyon, France
,
Anton Szymanowicz Laboratoire de Biochimie, Centre Hospitalier de Roanne, Roanne, France
,
Marie-Jeanne Neyron Laboratoire de Biochimie, Centre Hospitalier de Roanne, Roanne, France
,
Abdellah Zine Service de Pédiatrie, Centre Hospitalier de Roanne, Roanne, France
,
Henri Wajcman INSERM U 955, Hôpital Henri Mondor, Créteil, France
&
Alain Francina Unité de Pathologie Moléculaire du Globule Rouge, Fédération de Biochimie et de Biologie Spécialisée, Hôpital Edouard Herriot, Hospices Civils & Université Claude Bernard-Lyon 1, Lyon, FranceCorrespondence[email protected]
Pages 366-373 | Received 03 Feb 2010, Accepted 22 Feb 2010, Published online: 19 Jul 2010

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Thomas R. L. Klei, Sima Kheradmand Kia, Martijn Veldthuis, Javad Dehbozorgian, Mehran Karimi, Judy Geissler, Erica Sellink, Marijke Thiel-Valkhof, Patrick Burger, Floris van Alphen, Alexander B. Meijer, Robin van Bruggen & Rob van Zwieten. (2019) A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia. Hemoglobin 43:2, pages 77-82.
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