Evidence for a gene conversion in a Hb Arya Carrier [α codon 47 Asp>Asn, Hb A1(or Hb A2):c.142 G>A]

Author:

Pécriaux A.1,Paillard C.2,Galoisy A.3,Riou J.1,Le metayer N.1,Wajcman H.4,Pissard S.14

Affiliation:

1. Department of genetics; APHP, GHU Henri Mondor; Creteil France

2. Service d'hématologie oncologie pédiatrique; CHU Hautepierre and Laboratoire d'Immuno Rhumatologie Moléculaire; INSERM UMR_S1109; Faculté de Médecine; Fédération Hospitalo-Universitaire OMICARE; Fédération de Médecine Translationnelle de Strasbourg (FMTS); Université de Strasbourg; Strasbourg France

3. Laboratoire d'hématologie UF6344; CHU de Hautepierre; Strasbourg France

4. IMRB Inserm U 955eq2, and GReX; GHU Henri Mondor; Creteil France

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference9 articles.

1. Gene conversion: mechanisms, -evolution and human disease;Chen;Nat Rev Genet,2007

2. Pitfalls in the genetic diagnosis of Hb S;Moradkhani;Clin Biochem,2013

3. Hb Savaria [α49(CE7)Ser→Arg; HBA2: -c.150C>A]: a New Case and Complete Description;Tran Houangkeo;Hemoglobin,2016

4. Determining the cause of patchwork HBA1 and HBA2 genes: recurrent gene conversion or crossing over fixation events;Law;Haematologica,2006

5. A novel HBA2 gene conversion in cis or trans: -« α12 allele » in a Saudi population;Borgio;Blood Cells Mol Dis,2014

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