Title : Hereditary TP53 codon 292 and somatic P16INK4A codon 94 mutations in a Li-Fraumeni syndrome family.

Pub. Date : 1999 Sep

PMID : 10484981






1 Functional Relationships(s)
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1 In the analyses of tumor tissues from the propositus and his daughter, a P16INK4A codon 94 missense point mutation (GCG-->GAG; Ala-->Glu) was observed with the hereditary TP53 mutation. Alanine tumor protein p53 Homo sapiens