Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Genein Ciswith a −α3.7Thalassemia Deletion-Reference-Cited by-同舟云学术

Hb St. Jozef, A Val→Leu N-Terminal Mutation Leading to Retention of the Methionine, and Partial Acetylation Found in the Globin Genein Ciswith a −α3.7Thalassemia Deletion

Published:2007-01 Issue:3 Volume:31 Page:313-323
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Harteveld Cornelis L.,Versteegh Florens G.A.,van Leer Eduard H.G.,Starreveld Jaap S.,Kok Peter J.M.J.,van Rooijen-Nijdam Irene,van Delft Peter,Zanella-Cleon Isabelle,Becchi Michel,Wajcman Henri,Giordano Piero C.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/03630260701459473

Reference16 articles.

1. A complex haemoglobinopathy diagnosis in a family with both βo- and αo/+-thalassaemia homozygosity

2. Hb Amsterdam [α32(B13)Met→Ile (α2)]: A New Unstable Variant Associated with an α-Thalassemia Phenotype and a New African Polymorphism

3. Hb Oegstgeest [α104(G11)Cys → Ser (α1)]. A New Hemoglobin Variant Associated with a Mild α-Thalassemia Phenotype

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