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Hemoglobin
international journal for hemoglobin research
Volume 35, 2011 - Issue 2
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Short Communication

A Second Observation of the Rare Frameshift Mutation in the β-Globin Gene: Codon 46 (+A) (Hbb:c.138_139insA)

Elyes Slim Ghedira Laboratory of Biochemistry and Molecular Genetics, Henri Mondor Hospital (APHP), Creteil, France
,
Delphine Dupin-Deguine Department of Medical Genetics, Purpan Hospital, Toulouse France
,
Denis Duffilot Department of Pediatrics, Centre Hospitalier de Bigorre, Tarbes France
,
Nathalie Lemetayer Laboratory of Biochemistry and Molecular Genetics, Henri Mondor Hospital (APHP), Creteil, France
,
Emmanuelle Faubert Laboratory of Biochemistry and Molecular Genetics, Henri Mondor Hospital (APHP), Creteil, France
&
Serge Pissard Laboratory of Biochemistry and Molecular Genetics, Henri Mondor Hospital (APHP), Creteil, France; INSERM U955 eq.11, School of Medicine, Université Paris-Est Creteil (UPEC), Creteil, FranceCorrespondence[email protected]
Pages 157-161 | Received 23 Nov 2010, Accepted 07 Jan 2011, Published online: 21 Mar 2011

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Rakesh Kumar, Chandan Sagar, Dharmesh Sharma & Purnima Kishor. (2015) β-Globin Genes: Mutation Hot-Spots in the Global Thalassemia Belt. Hemoglobin 39:1, pages 1-8.
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Articles from other publishers (1)

R. Angalena, S. Aggarwal, S. R. Phadke & A. Dalal. (2012) Compound heterozygote condition in beta thalassemia major due to a novel single nucleotide deletion (-T) at codon 69 in association with IVS 1-5 (G>C) mutation. International Journal of Laboratory Hematology 34:4, pages e7-e9.
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