Title : A novel point mutation in the intracellular domain of the ret protooncogene in a family with medullary thyroid carcinoma.

Pub. Date : 1997 Dec

PMID : 9398735






1 Functional Relationships(s)
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1 In MEN 2B patients, a specific mutation at codon 918, substituting a threonine for a methionine, has been found in 95% of cases. Threonine ret proto-oncogene Homo sapiens