Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THEα1-GLOBIN CHAIN IS ASSOCIATED WITH A MILDα-THALASSEMIA PHENOTYPE-Reference-Cited by-同舟云学术

Hb GROENE HART: A NEW Pro→Ser AMINO ACID SUBSTITUTION AT POSITION 119 OF THEα1-GLOBIN CHAIN IS ASSOCIATED WITH A MILDα-THALASSEMIA PHENOTYPE

Published:2002-01 Issue:3 Volume:26 Page:255-260
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Harteveld Cornelis L.,Delft Peter van,Plug Rob,Versteegh Florens G.A.,Hagen Balt,Rooijen Irene van,Kok Peter J.M.J.,Wajcman Henri,Kister Jean,Giordano Piero C.

Publisher

Informa UK Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120015029

Reference9 articles.

1. Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method

2. A novel polyadenylation signal mutation in the α2-globin gene causing α thalassaemia

3. Human α‐Thalassemia syndromes: Detection of molecular defects

4. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia

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