HEMOPHILIA-A - DATABASE OF NUCLEOTIDE SUBSTITUTIONS, DELETIONS, INSERTIONS AND REARRANGEMENTS OF THE FACTOR-VIII GENE, 2ND EDITION (VOL 22,PG 3511, 1994)
A large number of different mutations in the factor VIII (F8) gene hav
e been identified as a cause of haemophilia A. This compilation lists
known single base-pair substitutions, deletions and insertions in the
F8 gene and reviews the status of the inversional events which account
for a substantial proportion of mutations causing severe haemophilia
A.