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
Establishing a comprehensive genetic diagnosis strategy for hemophilia B and its application in Chinese population.
Lin XY et al.
International Journal of Laboratory Hematology, 2018
[FⅨ gene all exons sequencing technology in hemophilia B gene carriers detection and the application of prenatal gene diagnosis].
Xiao X et al.
Zhonghua Xue Ye Xue Za Zhi = Zhonghua Xueyexue Zazhi, 2013
Analysis of F9 point mutations and their correlation to severity of haemophilia B disease.
Hamasaki-Katagiri N et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia, 2012
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