Associated Papers
Exploring gene editing as a potential therapeutic strategy for hemophilia.
Kumarasamy N et al.
Frontiers in Bioengineering and Biotechnology, 2026
Identification of Novel F9 Gene Variants in 143 Vietnamese Patients with Hemophilia B.
Bach KQ et al.
Journal of Blood Medicine, 2025
PAM-flexible Cas9-mediated base editing of a hemophilia B mutation in induced pluripotent stem cells.
Hiramoto T et al.
Communications Medicine, 2023
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
Investigation of killer cell immunoglobulin-like receptors KIR2DL2 and KIR2DL3 diversity and identification of ten novel KIR2DL3 alleles in the Chinese Han population.
He Y et al.
Scandinavian Journal of Immunology, 2015
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