SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. (Articolo in rivista)

Type
Label
  • SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Alternative label
  • 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. (2013)
    SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity.
    in Journal of bone and mineral research
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • 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. (literal)
Pagina inizio
  • 1041 (literal)
Pagina fine
  • 1049 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 28 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • IRGB/CNR e Humanitas Research Center (literal)
Titolo
  • SNX10 mutations define a subgroup of human autosomal recessive osteopetrosis with variable clinical severity. (literal)
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