A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α‐Thalassemia Deletions, in Three Independent Asian Cases-Reference-Cited by-同舟云学术

A New Hb Evanston Allele [α14(A12)Trp → Arg] Found Solely, and in the Presence of Common α‐Thalassemia Deletions, in Three Independent Asian Cases

Published:2004-01 Issue:1 Volume:28 Page:1-5
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Harteveld Cornelis L.,Wijermans Pierre W.,de Ree Juliette E. L. M.,Ter Hal Pauline,Van Delft Peter,Van Rooijen‐Nijdam Irene H.,Rasp Ellen,Kok Peter J. M. J.,Souverijn John H. M.,Versteegh Florens G. A.,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-120028881

Reference5 articles.

1. Molecular spectrum of ?-thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects

2. Hemoglobin Evanston (alpha 14 Trp----Arg). An unstable alpha-chain variant expressed as alpha-thalassemia.

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

4. Separation of Human Hemoglobins by Deae-Cellulose Chromatography using Glycine-Kcn-Nacl Developers

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

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