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. Teti*
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