Molecular analysis of eight severe FV-deficient patients in Pakistan: A large series of homozygous for frameshift mutations.
Munira BorhanyAlexandre RancMathilde FretignyGrégory MoulisMadiha AbidTahir ShamsiMuriel Giansily-BlaizotPublished in: Haemophilia : the official journal of the World Federation of Hemophilia (2019)