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

Author: Letizia C.  

Publisher: Springer Publishing Company

ISSN: 0171-967X

Source: Calcified Tissue International, Vol.74, Iss.1, 2004-01, pp. : 42-46

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Abstract