Secondary Mutation (c.94_95delAG) in A −α3.7Allele Associated with Hb H Disease in Two Unrelated African American Individuals Homozygous for the −α3.7Deletion (−α3.7/−α3.7T)-Reference-Cited by-同舟云学术

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Secondary Mutation (c.94_95delAG) in A −α3.7Allele Associated with Hb H Disease in Two Unrelated African American Individuals Homozygous for the −α3.7Deletion (−α3.7/−α3.7T)

Published:2011-12-21 Issue:1 Volume:36 Page:103-107
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Zhao Po,Buller-Burckle Arlene M.,Peng Mei,Anderson Alison,Han Z. Jenny,Gallivan Monica V.E.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2011.642915

Reference7 articles.

1. Hemoglobin H disease: not necessarily a benign disorder

2. Two New α-Thalassemia Frameshift Mutations

3. The Interaction of α-Thalassaemia and Haemoglobin G Philadelphia

4. Dinucleotide deletion in -α3.7allele causes a severe form of α+thalassaemia

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