Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis (Abstract in rivista)

Type
Label
  • Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis (Abstract in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Alternative label
  • A. Magariello, L. Citrigno, A. Patitucci, A. L. Gabriele, R. Mazzei1, F. L. Conforti, C. Ungaro, M. Caracciolo, W. Sproviero, A. Gambardella, M. Muglia (2011)
    Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • A. Magariello, L. Citrigno, A. Patitucci, A. L. Gabriele, R. Mazzei1, F. L. Conforti, C. Ungaro, M. Caracciolo, W. Sproviero, A. Gambardella, M. Muglia (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Institute of Neurological Sciences, CNR, Mangone (CS), Italy Department of Neurosciences, Psychiatric and Anesthesiological Sciences, University of Messina, Messina, Italy Institute of Neurology, University 'Magna Graecia, Catanzaro, Italy (literal)
Titolo
  • Receptor expression-enhancing protein 1 gene (SPG31) mutations are rare in Italian patients with hereditary spastic paraparesis (literal)
Prodotto di
Autore CNR

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