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Alessandra Pangrazio, Anders Fasth, Andrea Sbardellati, Paul J Orchard, Kimberly A Kasow, Jamal Raza, Canan Albayrak, Davut Albayrak, Olivier M Vanakker, Barbara De Moerloose, Ashok Vellodi, Luigi D Notarangelo, Claire Schlack, Gabriele Strauss, Jörn-Sven Kühl, Elena Caldana, Nadia Lo Iacono, Lucia Susani, Uwe Kornak, Ansgar Schulz, Paolo Vezzoni, Anna Villa and Cristina Sobacchi SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity Journal of Bone and Mineral Research 28

Article first published online: 17 APR 2013 | DOI: 10.1002/jbmr.1849

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