Orphanet - Il portale delle malattie rare e dei farmaci orfani: “The CLN8 variant late-infantile neuronal ceroid lipofuscinosis (CLN8-vLINCL): functional aspects of the CLN8 protein and characterization of the degenerative mechanisms”. (Risultati di valorizzazione applicativa)

Type
Label
  • Orphanet - Il portale delle malattie rare e dei farmaci orfani: “The CLN8 variant late-infantile neuronal ceroid lipofuscinosis (CLN8-vLINCL): functional aspects of the CLN8 protein and characterization of the degenerative mechanisms”. (Risultati di valorizzazione applicativa) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Alternative label
  • Guarneri P. (2010)
    Orphanet - Il portale delle malattie rare e dei farmaci orfani: “The CLN8 variant late-infantile neuronal ceroid lipofuscinosis (CLN8-vLINCL): functional aspects of the CLN8 protein and characterization of the degenerative mechanisms”.
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Guarneri P. (literal)
Titolo
  • Orphanet - Il portale delle malattie rare e dei farmaci orfani: “The CLN8 variant late-infantile neuronal ceroid lipofuscinosis (CLN8-vLINCL): functional aspects of the CLN8 protein and characterization of the degenerative mechanisms”. (literal)
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Autore CNR

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