A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome

✍ Scribed by Giacché, M.; Panarotto, A.; Mori, L.; Daffini, L.; Tacchetti, M. C.; Pirola, I.; Agabiti Rosei, E.; Castellano, M.

• Book ID: 125335987
• Publisher: Springer-Verlag
• Year: 2012
• Tongue: English
• Weight: 124 KB
• Volume: 35
• Category: Article
• ISSN: 0391-4097
• DOI: 10.1007/BF03345419