Associated Papers
Molecular Genetic Analysis of Russian Patients with Coagulation Factor FVII Deficiency.
Pshenichnikova O et al.
Genes, 2023
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effect.
Sharma R et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2023
The EAHAD blood coagulation factor VII variant database.
Giansily-Blaizot M et al.
Human Mutation, 2020
Two new double mutant alleles of the F7 gene and a literature review on alleles with two mutations in FVII deficiency.
Giansily-Blaizot M et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2016
The molecular basis of low activity levels of coagulation factor VII: a Brazilian cohort.
Rabelo FY et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2015
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