SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.
Pangrazio A, Fasth A, Sbardellati A, Orchard PJ, Kasow KA, Raza J, Albayrak C, Albayrak D, Vanakker OM, De Moerloose B, Vellodi A, Notarangelo LD, Schlack C, Strauss G, Kühl JS, Caldana E, Lo Iacono N, Susani L, Kornak U, Schulz A, Vezzoni P, Villa A, Sobacchi C.
Pangrazio A, et al. Among authors: strauss g.
J Bone Miner Res. 2013 May;28(5):1041-9. doi: 10.1002/jbmr.1849.
J Bone Miner Res. 2013.
PMID: 23280965
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