Snx10: a newly identified locus associated with human osteopetrosis
- PMID: 25419438
- PMCID: PMC4237201
- DOI: 10.1038/bonekey.2013.155
Snx10: a newly identified locus associated with human osteopetrosis
Conflict of interest statement
The authors declare no conflict of interest.
Figures
References
-
- Aker M, Rouvinski A, Hashavia S, Ta-Shma A, Shaag A, Zenvirt S, et al. An SNX10 mutation causes malignant osteopetrosis of infancy. J Med Genet. 2012;49:221–226. - PubMed
-
- Zhu CH, Morse LR, Battaglino RA. SNX10 is required for osteoclast formation and resorption activity. J Cell Biochem. 2012;113:1608–1615. - PubMed
-
- Mégarbané A, Pangrazio A, Villa A, Chouery E, Maarawi J, Sabbagh S, et al. Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia. Eur J Med Genet. 2013;56:32–35. - PubMed
-
- Pangrazio A, Fasth A, Sbardellati A, Orchard PJ, Kasow KA, Raza J, et al. SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. J Bone Miner Res. 2013;28:1041–1049. - PubMed
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources