α+-Thalassemia Trait Caused by a Nonsense Mutation in the α2-Globin Gene: Codon 54 (CAG>TAG)
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260802625980
Reference9 articles.
1. A rapid and reliable 7-deletion multiplex polymerase chain reaction assay for α-thalassemia
2. Locus assignment of human a globin mutations by selective amplification and direct sequencing
3. Nonsense-mediated mRNA decay modulates clinical outcome of genetic disease
4. Molecular spectrum of ?-thalassemia in the Iranian population of Hormozgan: Three novel point mutation defects
5. A Novel α‐Thalassemia Nonsense Mutation in Codon 23 of the α2‐Globin Gene (GAG→TAG) in a Tunisian Family
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1. In vitroCharacterization of the α-Thalassemia Point Mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)];Hemoglobin;2011-10-03
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