Associated Papers
Molecular mechanism of a novel Ser362Asn mutation causing inherited FX deficiency in a Chinese family.
Zhang X et al.
International Journal of Hematology, 2020
A novel Ala275Val mutation in factor X gene influences its structural compatibility and impairs intracellular trafficking and coagulant activity.
Sun N et al.
Thrombosis Research, 2016
Molecular basis of factor X deficiency cases from India.
Mota L et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2010
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