CDKN2B

Hereditary familial melanoma, 9p21 locus without CDKN2A coding variant

1 article(s) in the watch · Cancer genetics

Curated publications

Disruption of CTCF binding by germline non-coding variants in CDKN2B suppress CDKN2B expression in melanoma-prone families

Hereditary familial melanoma, 9p21 locus without CDKN2A coding variant

Automatic aggregation page — a clinical introduction may be added.