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Familial non-multiple endocrine neoplasia medullary thyroid carcinoma: Report of a case confirming a new clinical entity in Japan

✍ Scribed by Makoto Katagiri; Takahiro Ohtawa; Kunihiko Ito; Tanekazu Harada


Book ID
112290157
Publisher
Springer
Year
1995
Tongue
English
Weight
387 KB
Volume
25
Category
Article
ISSN
1436-2813

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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