Associated Papers
Genetic variant detection in a South African haemophilia B population.
Bester C et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2024
Compensatory epistasis explored by molecular dynamics simulations.
Serrano C et al.
Human Genetics, 2021
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
Hemophilia B: molecular pathogenesis and mutation analysis.
Goodeve AC
Journal of Thrombosis and Haemostasis : Jth, 2015
25851415 (PubMed )
Supplement: JTH-13-1184-s001.docx
An interactive mutation database for human coagulation factor IX provides novel insights into the phenotypes and genetics of hemophilia B.
Rallapalli PM et al.
Journal of Thrombosis and Haemostasis : Jth, 2013
Mutations in pimE restore lipoarabinomannan synthesis and growth in a Mycobacterium smegmatis lpqW mutant.
Crellin PK et al.
Journal of Bacteriology, 2008
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