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*
*Corresponding author for this work
Research output: Contribution to journal › Article › peer-review
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