Associated Papers
Novel biallelic CDK9 variants are associated with retinal dystrophy without CHARGE-like malformation syndrome.
Nishina S et al.
Journal of Human Genetics, 2026
Biallelic CDK9 variants as a cause of a new multiple-malformation syndrome with retinal dystrophy mimicking the CHARGE syndrome.
Nishina S et al.
Journal of Human Genetics, 2021
CanDrA: cancer-specific driver missense mutation annotation with optimized features.
Mao Y et al.
Plos One, 2013
24205039 (PubMed )
Supplement: pone.0077945.s001.xls › Table_S4
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