Molecular identification of rare FY*Null and FY*X alleles in Caucasian thalassemic family from Sardinia
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference18 articles.
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4. The Fyx phenotype is associated with a missense mutation in the Fyb allele predicting Arg89Cys in the Duffy glycoprotein;Olsson;Br J Haematol,1998
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1. The highest Duffy (FYX) allele frequency ever reported for Scottish population: A cross‐sectional study;Health Science Reports;2023-06
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