Hb Sallanches [α104(G11)Cys→Tyr, TGC→TAC (α2)]: An Unstable Hemoglobin Variant Found in an Indian Child
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260600755872
Reference5 articles.
1. Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia
2. A new α chain variant Hb Sallanches [α2 104(G11) Cys→Tyr] associated with HbH disease in one homozygous patient
3. Homozygous HB Sallanches [α104(G11)CYS→TYR] in a Pakistani Child with HB H Disease
4. Hb Sallanches [α104(G11)Cys→Tyr]: A Rare α2-Globin Chain Variant Found in the Homozygous State in Three Members of a Pakistani Family
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1. Molecular Heterogeneity of Hb H Disease in India;Thalassemia Reports;2022-07-06
2. 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
3. Molecular Diversity of Hemoglobin H Disease in India: Table 1;American Journal of Clinical Pathology;2010-03
4. Hb H Disease Due to Homozygosity for a Rare α2-Globin Variant, Hb Sallanches;Hemoglobin;2010-01
5. Hb Sallanches [α104(G11)Cys→Tyr, TGC>TAC] Occurs Frequently on the Indian Subcontinent;Hemoglobin;2009-12
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