Medullary thyroid carcinoma (MTC) may occur sporadically or as part of the autosomal dominant multiple endocrine neoplasia type 2 (MEN 2). Three hereditary forms of MEN 2 have been identified: MEN 2A, MEN 2B, and familial MTC (FMTC). Missense germ-line mutations in the RET protooncogene have been id
β¦ LIBER β¦
The newly detected mutations in theRETproto-oncogene in exon 16 as a cause of sporadic medullary thyroid carcinoma
β Scribed by S. Jindrichova; R. Kodet; L. Krskova; P. Vlcek; B. Bendlova
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 229 KB
- Volume
- 81
- Category
- Article
- ISSN
- 0946-2716
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