Identification of three novel menin mutations (c.741delGTCA, c.1348T>C, c.1785delA) in unrelated Italian families affected with multiple endocrine neoplasia type 1: Additional information for mutational screening

✍ Scribed by C. Asteria; G. Faglia; R. Roncoroni; G. Borretta; P. Ribotto; P. Beck-Peccoz

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 20 KB
• Volume: 17
• Category: Article
• ISSN: 1059-7794
• DOI: 10.1002/humu.12