HB F-Yamaguchi (γ75THR, γ80ASN, γ136ALA) is associated withGγ-thalassemia
Author:
Publisher
Wiley
Subject
Hematology
Reference8 articles.
1. Survey of cord blood Hemoglobin in Japan and Identification of two new γ Chain Variants
2. Alpha chain and gamma chain abnormal hemoglobins in newborn babies: Structural and genetic aspects
3. Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes
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1. Identical Mutations in the Paralogous Human γ-Globin Genes Leading to Hemoglobin Variants and Nondeletional Hereditary Persistence of Fetal Hemoglobin;Hemoglobin;2011-03-21
2. Disorders of the synthesis of human fetal hemoglobin;IUBMB Life;2008
3. Hb F‐Porto Torres [Aγ75(E19)Ile→Thr, 136(H14)Ala→Ser]: A Novel Variant of theAγ Chain Having Two Substitutions, One Being that of Hb F‐Sardinia;Hemoglobin;2004-01
4. Structural Alterations of the γ‐Globin Genes in a Brazilian Population;Hemoglobin;2004-01
5. Gamma chain abnormal human fetal hemoglobin variants;American Journal of Hematology;1997-07
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