From: First report of molecular diagnosis of Tunisian hemophiliacs A: Identification of 8 novel causative mutations
Family
Number of Patient
FVIII:C
Intron 22 Inversion
Type I
Type II
Other Type
Family 8
1
<1%
Yes: 18 kb, 15.5 kb and 14 kb
Family 9
2
Yes
Family 10
Family 11
yes
Family 12