A rare mutation [IVS-1-130 (G-A)] in a Turkish β-thalassemia major patient

American Journal of Hematology

Volumn 63, Issue 4, 2000, Pages 223-225

  Tadmouri, G O ^a   Bilenoglu O ^a   Kantarci, S ^b   Kayserili, H ^c   Perrin, P ^d   Başak, A Nazli ^a  

^a BOGAZICI UNIVERSITY   (Turkey)

^b Duzen Laboratories   (Turkey)

^c ISTANBUL UNIVERSITY   (Turkey)

^d CENTRE DE GÉNÉTIQUE MOLÉCULAIRE ET CELLULAIRE   (France)

Author keywords

thalassemia; Haplotype; North Africa; Rare mutation; Turkey

Indexed keywords

ARTICLE; CASE REPORT; DNA DETERMINATION; FEMALE; GENE MUTATION; GENETIC POLYMORPHISM; GLOBIN GENE; HAPLOTYPE; HUMAN; NORTH AFRICA; PRESCHOOL CHILD; PRIORITY JOURNAL; SEQUENCE ANALYSIS; THALASSEMIA MAJOR; TURKEY (REPUBLIC);

ALBANIA; ALLELES; BETA-THALASSEMIA; CHILD, PRESCHOOL; FAMILY HEALTH; FEMALE; HAPLOTYPES; HUMANS; POINT MUTATION; TURKEY;

EID: 17644449318     PISSN: 03618609     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8652(200004)63:4<223::AID-AJH10>3.0.CO;2-B     Document Type: Article

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