Molecular etiology of factor VIII deficiency in hemophilia A
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference121 articles.
1. Two Novel Mutations at 373 Codon of FVIII Gene Detected by DGGE
2. A new Hind III restriction fragment length polymorphism in the hemophilia A locus
3. Hemophilia A due to mutations that create new N-glycosylation sites.
4. The molecular basis of hemophilia A in man
5. (1992) Hemophilias. In (eds): “Prenatal Diagnosis and Scrcening.” Edinburgh: Churchill Livingstone, pp 477-481.
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