✦ LIBER ✦

Biochemical diagnosis, localization and management of pheochromocytoma: focus on multiple endocrine neoplasia type 2 in relation to other hereditary syndromes and sporadic forms of the tumour

✍ Scribed by K. PACAK; I. ILIAS; K. T. ADAMS; G. EISENHOFER

Book ID: 108861984
Publisher: John Wiley and Sons
Year: 2005
Tongue: English
Weight: 192 KB
Volume: 257
Category: Article
ISSN: 0954-6820
DOI: 10.1111/j.1365-2796.2004.01425.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutations of the RET proto-oncogene in t

Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease

✍ Charis Eng; Lois M. Mulligan 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 225 KB 👁 2 views

## Communicated by Martin Bobrow The RET proto-oncogene codes for a receptor tyrosine kinase thought to play a role in the development of neural crest and its derivatives. Mutations in the RET proto-oncogene have been found in patients with the multiple endocrine neoplasia type 2 syndromes (MEN 2)