Associated Papers
Molecular analysis of 76 Chinese hemophilia B pedigrees and the identification of 10 novel mutations.
Huang L et al.
Molecular Genetics & Genomic Medicine, 2020
Splicing dysregulation contributes to the pathogenicity of several F9 exonic point variants.
Katneni UK et al.
Molecular Genetics & Genomic Medicine, 2019
31257730 (PubMed )
Supplement: MGG3-7-e840-s002.xls › F9_Splicing_Data
A K19E missense mutation in the plasminogen gene is a common cause of familial hypoplasminogenaemia.
Tefs K et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2003
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