Associated Papers
Therapeutic base editing to generate a gain-of-function F9 variant for hemophilia B.
Baatartsogt N et al.
Blood, 2026
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
The State of Skewed X Chromosome Inactivation is Retained in the Induced Pluripotent Stem Cells from a Female with Hemophilia B.
Lyu C et al.
Stem Cells and Development, 2017
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