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Association of mitochondrial DNA transversion mutations with familial medullary thyroid carcinoma/multiple endocrine neoplasia type 2 syndrome

✍ Scribed by Abu-Amero, K K; Alzahrani, A S; Zou, M; Shi, Y


Book ID
110070128
Publisher
Nature Publishing Group
Year
2005
Tongue
English
Weight
193 KB
Volume
25
Category
Article
ISSN
0950-9232

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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