Type II Benign Osteopetrosis (Albers-Schönberg Disease) Caused by a Novel Mutation in CLCN7 Presenting with Unusual Clinical Manifestations
Titel:
Type II Benign Osteopetrosis (Albers-Schönberg Disease) Caused by a Novel Mutation in CLCN7 Presenting with Unusual Clinical Manifestations
Auteur:
Letizia, C. Taranta, A. Migliaccio, S. Caliumi, C. Diacinti, D. Delfini, E. D’Erasmo, E. Iacobini, M. Roggini, M. Albagha, O. M. E. Ralston, S. H. Teti, A.