A Novel Mutation of the α2-Globin Causing α -Thalassemia: Hb Plasencia [α125(H8)Leu→Arg (α2)-Reference-Cited by-同舟云学术

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A Novel Mutation of the α2-Globin Causing α -Thalassemia: Hb Plasencia [α125(H8)Leu→Arg (α2)

Published:2005-05-01 Issue:2 Volume:29 Page:113-117
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:LHEM

Author:

Martin Guillermo,Villegas Ana,González Fernando Ataulfo,Ropero Paloma,Hojas Ricardo,Polo Marta,Mateo Marta,Salvador Maria,Benavente Celina

Publisher

Informa UK Limited

Subject

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

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Novel Mutation at HBA1: c.349G>T Causing α-Thalassemia in a Chinese Family;Hemoglobin;2021-06-04

2. In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia;Hemoglobin;2020-03-03

3. Hb Plasencia [α125(H8)Leu→Arg (α2)] is a Frequent Cause ofα+-Thalassemia in the Portuguese Population;Hemoglobin;2013-01-31

4. Hb Iberia [α104(G11)Cys → Arg,TGC>CGC (α2) (HBA2:c.313T>C)], a Newα-Thalassemic Hemoglobin Variant Found in the Iberian Peninsula: Report of Six Cases;Hemoglobin;2012-08

5. A Dyserythropoietic Anemia Associated with Homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), A Variant with an Unstable α Chain;Hemoglobin;2010-11-15

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