Type II Benign Osteopetrosis (Albers-Schönberg Disease) Caused by a Novel Mutation in CLCN7 Presenting with Unusual Clinical Manifestations

✍ Scribed by C. Letizia; A. Taranta; S. Migliaccio; C. Caliumi; D. Diacinti; E. Delfini; E. D’Erasmo; M. Iacobini; M. Roggini; O. M. E. Albagha; S. H. Ralston; A. Teti

• Book ID: 105913043
• Publisher: Springer
• Year: 2003
• Tongue: English
• Weight: 179 KB
• Volume: 74
• Category: Article
• ISSN: 1432-0827
• DOI: 10.1007/s00223-002-1087-5