Hb Angers: A new α2‐globin variant [α2 (140)(HC2) Tyr → Ser; HBA2 : C.422 A>C] with increased oxygen affinity leading to erythrocytosis

Author:

Orvain Corentin123ORCID,Kiger Laurent4,Peronet Isabelle5,Peron Anne5,Galacteros Frederic46ORCID,Wajcman Henri4,Pissard Serge45ORCID

Affiliation:

1. Maladies du Sang CHU d’Angers Angers France

2. Fédération Hospitalo‐Universitaire Grand‐Ouest Acute LeukemiaFHU‐GOAL Angers France

3. CRCINAINSERM 1232 Angers France

4. Inserm‐U955eq2 and LabEx GreX Univ Paris Est Creteil, INSERM‐U955, IMRB, F‐94010 Creteil, France and CréteilF‐94010France

5. Département de Génétique Moléculaire Hopital Universitaire H. MondorAP‐HP CréteilF‐94010France

6. Unité des Maladies Génétiques du Globule Rouge Centre de Référence des Pathologies du Globule Rouge APHPHôpital Universitaire H. Mondor CréteilF‐94010France

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference12 articles.

1. The complete evaluation of erythrocytosis: congenital and acquired

2. Congenital polycythemias/erythrocytoses;Gordeuk VR;Haematologica,2005

3. Hemoglobins With High Oxygen Affinity Leading to Erythrocytosis. New Variants and New Concepts

4. Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases

5. Diagnostic approach to hemoglobins with high oxygen affinity: experience from France and Belgium and review of the literature;Orvain C;Ann Biol Clin (Paris),2017

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