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A New Hot Spot for Mutations in the ret Protooncogene Causing Familial Medullary Thyroid Carcinoma and Multiple Endocrine Neoplasia Type 2A

โœ Scribed by Berndt, I.


Book ID
121358606
Publisher
Endocrine Society
Year
1998
Tongue
English
Weight
451 KB
Volume
83
Category
Article
ISSN
0021-972X

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Communicated by Kenneth K. Kidd Gennline missense mutations within the coding region of the RET proto-oncogene have recently been described in patients with the dominantly inherited cancer syndromes, multiple endocrine neoplasia type 2a (MEN 2a) and familial medullary thyroid carcinoma (FMTC). To da