Hb Prato α31(B12)Arg→ser] in a Calabrian Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269208998868
Reference7 articles.
1. A new abnormal human hemoglobin: Hb prato (α231 (B12) Arg→Ser β2)
2. A Simple Method for the Detection of Unstable Haemoglobins
3. Rapid electrophoresis and quantitation of haemoglobins on cellulose acetate
4. Abnormal human haemoglobins
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1. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand;Hemoglobin;2020-07-03
2. In SilicoAnalysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia;Hemoglobin;2020-03-03
3. Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein;Blood;2009-06-04
4. Hb Prato [α31(B12)Arg→Ser (α2)] and α‐Thalassemia in a Taiwanese;Hemoglobin;2003-01
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