The Codon 35 (A > G) (HBB: c.107A > G) at theα-βChain Interface of theβ-Globin Gene: A Silent Mutation?
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269.2015.1099547
Reference6 articles.
1. The Molecular Basis of -Thalassemia
2. Hemoglobin Variants: Biochemical Properties and Clinical Correlates
3. A novel beta-globin mutation (HBB:c.107A>G; or codon 35 β (A→G)) at alpha–beta chain interfaces
4. Molecular Stability of he Philly (α2β235 (C1) Tyr → Phe)
5. The artificial α1β1-contact mutant hemoglobin, Hb Phe-35β, shows only small functional abnormalities
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