Title : Identification of a novel point mutation in the RET gene (Ala883Thr), which is associated with medullary thyroid carcinoma phenotype only in homozygous condition.

Pub. Date : 2004 Nov

PMID : 15531548






1 Functional Relationships(s)
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1 We describe here a novel germline homozygous mutation in exon 15 of the RET gene that determines an amino acid substitution (Ala->Thr) at codon 883. Threonine ret proto-oncogene Homo sapiens