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RET mutation profile and variable clinical manifestations in a family with multiple endocrine neoplasia type 2A and Hirschsprung's disease

✍ Scribed by Pasini, Barbara; Rossi, Roberta; Ambrosio, Maria Rosaria; Zatelli, Maria Chiara; Gullo, Maria; Gobbo, Morena; Collini, Paola; Aiello, Antonella; Pansini, Giancarlo; Trasforini, Giorgio; Uberti, Ettore Ciro degli

Book ID: 122372389
Publisher: Elsevier Science
Year: 2002
Tongue: English
Weight: 111 KB
Volume: 131
Category: Article
ISSN: 0039-6060
DOI: 10.1067/msy.2002.121093

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## 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)