A Dyserythropoietic Anemia Associated with Homozygous Hb Plasencia [α125(H8)Leu→Arg (α2)] (HBA2:c.377T>G), A Variant with an Unstable α Chain-Reference-Cited by-同舟云学术

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

Published:2010-11-15 Issue:6 Volume:34 Page:576-581
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Garçon Loïc,Iolascon Achille,Pissard Serge,Esposito Maria R.,Russo Roberta,Fenneteau Odile,Fénéant-Thibault Madeleine,Heimpel Hermann,Delaunay Jean

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269.2010.526922

Reference22 articles.

1. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II

2. Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in theSEC23Bgene

3. A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis

Cited by 3 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. MISCELLANEOUS DISORDERS;Bone Marrow Pathology;2019-03-08

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

3. 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

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