Title : A Korean family of familial medullary thyroid cancer with Cys618Ser RET germline mutation.

Pub. Date : 2010 Feb

PMID : 20119574






2 Functional Relationships(s)
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1 We report a RET mutation in exon10, codon 618 that causes substitution of a cysteine by a serine in the cysteine-rich domain of the RET receptor in a three-generation FMTC family composed of 30 members with 11 carriers. Serine ret proto-oncogene Homo sapiens
2 We report a RET mutation in exon10, codon 618 that causes substitution of a cysteine by a serine in the cysteine-rich domain of the RET receptor in a three-generation FMTC family composed of 30 members with 11 carriers. Serine ret proto-oncogene Homo sapiens