Genetic studies suggest a multicentric origin for Hb G-Coushatta [β22(B4)Glu→Ala]

Hemoglobin

Volumn 23, Issue 1, 1999, Pages 57-67

  Li, J ^a   Wilson, D ^a   Plonczynski, M ^a   Harrell, A ^a   Cook, C B ^b   Scheer, W D ^b   Zeng, Y T ^c   Coleman, M B ^a   Steinberg, M H ^a,b  

^a VETERANS AFFAIRS MEDICAL CENTER   (United States)

^b UNIVERSITY OF MISSISSIPPI   (United States)

^c Shanghai Institute of Medical Genetics   (China)

Author keywords

Abnormal hemoglobin (Hb); Globin gene; Haplotype

Indexed keywords

ALANINE; GLUTAMIC ACID; HEMOGLOBIN VARIANT; UNCLASSIFIED DRUG;

ARTICLE; CODON; GENE CLUSTER; GENE CONVERSION; GENE MUTATION; GENETIC POLYMORPHISM; GLOBIN GENE; HAPLOTYPE; HEMOGLOBIN DETERMINATION; HEMOGLOBIN G COUSHATTA; HETEROZYGOSITY; HUMAN;

EID: 0032992680     PISSN: 03630269     EISSN: None     Source Type: Journal    
DOI: 10.3109/03630269908996148     Document Type: Article

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