## Abstract The inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN 2) is caused by mutations of the RET receptor tyrosine kinase and is characterized by medullary thyroid carcinoma. MEN 2 subtypes have distinct mutational spectrums and vary in severity. The most severe disease subty
✦ LIBER ✦
RET is expressed but not mutated in extra-adrenal paragangliomas
✍ Scribed by Ronald R. de Krijger; Erwin van der Harst; Seraina Muletta-Feurer; Hajo A. Bruining; Steven W. J. Lamberts; Winand N. M. Dinjens; Jürgen Roth; Philipp U. Heitz; Paul Komminoth
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 149 KB
- Volume
- 191
- Category
- Article
- ISSN
- 0022-3417
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