Title : RET proto-oncogene: a review and update of genotype-phenotype correlations in hereditary medullary thyroid cancer and associated endocrine tumors.

Pub. Date : 2005 Jun

PMID : 16029119






1 Functional Relationships(s)
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1 Mutations in six exons (10, 11, 13, 14, 15, and 16) located in either cysteine-rich or tyrosine kinase domains cause one of three distinctive clinical subtypes: familial MTC, multiple endocrine neoplasia (MEN) type 2A (including variants with Hirschsprung"s disease and cutaneous lichen amyloidosis), and MEN 2B. Cysteine ret proto-oncogene Homo sapiens