SNX10 mutations define a subgroup of human Autosomal Recessive Osteopetrosis with variable clinical severity.

Références BibTex

@Article{PFSOKRAAVDVNSSKCLSKSVVS13,
  author       = {Pangrazio, A. and Fasth, A. and Sbardellati, A. and Orchard, P. and Kasow, K. and Raza, J. and Albayrak, C. and Albayrak, D. and Vanakker, O. and De Moerloose, B. and Vellodi, A. and Notarangelo, L. and Schlack, C. and Strauss, G. and Kuhl, J.-S. and Caldana, E. and Lo Iacono, N. and Susani, L. and Kornak, U. and Schulz, A. and Vezzoni, P. and Villa, A. and Sobacchi, C.},
  title        = {SNX10 mutations define a subgroup of human Autosomal Recessive Osteopetrosis with variable clinical severity.},
  journal      = {Journal of Bone and Mineral Research},
  number       = {5},
  volume       = {28},
  pages        = {1041–1049},
  month        = {april},
  year         = {2013},
  publisher    = {Wiley},
  note         = {The manuscript has been  definitely accepted for publication in JBMR.},
  keywords     = {SNX10 Osteopetrosis homology model},
  doi          = {10.1002/jbmr.1849},
  url          = {https://publications.crs4.it/pubdocs/2013/PFSOKRAAVDVNSSKCLSKSVVS13},
}

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