Harvard Catalyst Profiles

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SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.

SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. J Bone Miner Res. 2013 May; 28(5):1041-9.

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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.