A new Unstable α2‐Globin Gene Variant: Hb Chartres [α33(B14)Phe→Ser]
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1081/HEM-120021544
Reference12 articles.
1. ABNORMAL HEMOGLOBINS: LABORATORY METHODS
2. Hb DOUALA [α3(A1)Ser → Phe]: A NEW α1 GENE MUTATION IN A CAMEROONIAN WOMAN HETEROZYGOUS FOR Hb S AND A 3.7 kb DELETIONAL α-THALASSEMIA
3. Cavities in proteins: structure of a metmyoglobin xenon complex solved to 1.9 .ANG.
4. The role of cavities in protein dynamics: Crystal structure of a photolytic intermediate of a mutant myoglobin
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2. Variable and Often Severe Phenotypic Expression in Patients with the α-Thalassemic Variant Hb Agrinio [α29(B10)Leu→Pro (α2)];Hemoglobin;2010-09-20
3. Further Identification of The Hyperunstable α-Globin Chain Variant Hb Heraklion [codons 36/37 (–CCC); Pro→0 (α1)] in Greek Cases With Co-Inherited α+-Thalassemia Mutations;Hemoglobin;2008-01
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