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Type II Benign Osteopetrosis (Albers-Schönberg Disease) Caused by a Novel Mutation in CLCN7 Presenting with Unusual Clinical Manifestations
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. TetiVolume:
74
Language:
english
Pages:
5
DOI:
10.1007/s00223-002-1087-5
Date:
January, 2004
File:
PDF, 179 KB
english, 2004