Characterization of mutations within the factor VIII gene of 73 unrelated mild and moderate haemophiliacs
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1995.tb05322.x/fullpdf
Reference37 articles.
1. Hemophilia A due to mutations that create new N-glycosylation sites.
2. A past mutation at Isoleucine397is now a common cause of moderate/mild haemophilia B
3. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.
4. Amino acid substitutions in conserved domains of factor VIII and related proteins: Study of patients with mild and moderately severe hemophilia A
5. Detection of mutations in the factor VIII gene using single-stranded conformational polymorphism (SSCP)
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