Compound heterozygous mutations (p.Leu13Pro and p.Tyr294*) associated with factor VII deficiency cause impaired secretion through ineffective translocation and extensive intracellular degradation of factor VII
Keywords: A; adenine; Arg; arginine; ASRA; allele-specific restriction enzyme analysis; C; cytosine; cDNA; complementary deoxyribonucleic acid; CHO; Chinese hamster ovary; DMEM; Dulbecco's modified Eagle medium; EGF; epidermal growth factor; ELISA; enzyme-linked im