Associated Papers
Mutation analysis and characterisation of F9 gene in haemophilia- B population of India.
Kulkarni S et al.
Blood Research, 2021
Molecular classification of blood and bleeding disorder genes.
Baz B et al.
Npj Genomic Medicine, 2021
34272389 (PubMed )
Supplement: 41525_2021_228_MOESM1_ESM.pdf
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
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