Associated Papers
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
Genetic analysis of a hemophilia B family with a novel F9 gene mutation: A STROBE-compliant article.
Lv X et al.
Medicine, 2019
Hemophilia B: molecular pathogenesis and mutation analysis.
Goodeve AC
Journal of Thrombosis and Haemostasis : Jth, 2015
25851415 (PubMed )
Supplement: JTH-13-1184-s001.docx
Mild haemophilia B from a novel missense mutation Ser350Ala of the F9 gene.
Park CH et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis, 2013
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