Heterozygosity for the IVS-I-5(G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Djonburi) in trans resulting in a thalassemia intermedia-Reference-Cited by-同舟云学术

Heterozygosity for the IVS-I-5(G→C) mutation with a G→A change at codon 18 (Val→Met; Hb Baden) in cis and a T→G mutation at codon 126 (Val→Gly; Hb Djonburi) in trans resulting in a thalassemia intermedia

Published:1992-12 Issue:2 Volume:1180 Page:173-179
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Divoky Vladimir,Bissé Emmanuel,Wilson Jerry B.,Gu Li-Hao,Wieland Heinrich,Heinrichs Irene,Prior John F.,Titus H.J. Huisman

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

Reference28 articles.

1. Hemoglobin: Molecular, Genetic and Clinical Aspects;Bunn,1986

2. The β- and δ-Thalassemia Repository

3. The Hemoglobinopathies Techniques of Identification;Huisman,1977

4. The Hemoglobinopathies;Righetti,1986

5. High-performance liquid chromatographic separation of human haemoglobins

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