Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression
Author:
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/57/4/705/583553/705.pdf
Cited by 46 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. In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia;Hemoglobin;2020-03-03
2. Molecular diagnosis of α-thalassemia in a multiethnic population;European Journal of Haematology;2017-04-06
3. Description of Three NewαVariants and Four NewβVariants: Hb Montluel [α110(G17)Ala → Val;HBA1: c.332C > T], Hb Cap d’Agde [α131(H14)Ser → Cys;HBA2: c.395C > G] and Hb Corsica [α100(G7)Leu → Pro;HBA1: 302T > C]; Hb Nîmes [β104(G6)Arg → Gly;HBB: c.313A > G], Hb Saint Marcellin [β112(G14)Cys → Gly;HBB: c.337T > G], Hb Saint Chamond [β80(EF4)Asn → 0;HBB: c.241_243delAAC] and Hb Dompierre [β29(B11)Gly → Arg;HBB: c.88G > C];Hemoglobin;2015-05-04
4. 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
5. α-thalassaemia;Orphanet Journal of Rare Diseases;2010-05-28
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