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The familial medullary thyroid carcinoma-associated RET E768D mutation in a multiple endocrine neoplasia type 2A case

✍ Scribed by Antonella Aiello; Katia Cioni; Morena Gobbo; Paola Collini; Maria Gullo; Gabriella Della Torre; Emanuele Passerini; Barbara Ferrando; Silvana Pilotti; Marco A. Pierotti; Barbara Pasini


Book ID
113920016
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
285 KB
Volume
137
Category
Article
ISSN
0039-6060

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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