LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease (Articolo in rivista)

Type
Label
  • LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1111/j.1399-0004.2007.00771.x (literal)
Alternative label
  • D. Civitelli; P. Tarantino; G. Nicoletti; I.C. Cirò Candiano; F. Annesi; E.V. De Marco; S. Carrideo; F.E. Rocca; F. Condino; P. Spadafora; P. Pugliese; S. D'Asero; M. Morelli; S. Paglionico; G. Annesi;A. Quattrone. (2007)
    LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease
    in Clinical genetics
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • D. Civitelli; P. Tarantino; G. Nicoletti; I.C. Cirò Candiano; F. Annesi; E.V. De Marco; S. Carrideo; F.E. Rocca; F. Condino; P. Spadafora; P. Pugliese; S. D'Asero; M. Morelli; S. Paglionico; G. Annesi;A. Quattrone. (literal)
Pagina inizio
  • 367 (literal)
Pagina fine
  • 370 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 71 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • D Civitelli: Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy P Tarantino:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy G Nicoletti:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy IC Ciro` Candiano:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy F Annesia:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy EV De Marco:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy S Carrideo:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy FE Rocca:Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy F Condino: Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy P Spadafora: Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy P Pugliese: Institute of Neurology, Department of Medical Sciences, University Magna Graecia, Catanzaro, Italy S D'Asero: Institute of Neurology, Department of Medical Sciences, University Magna Graecia, Catanzaro, Italy M Morelli: Institute of Neurology, Department of Medical Sciences, University Magna Graecia, Catanzaro, Italy S Paglionico: Institute of Neurology, Department of Medical Sciences, University Magna Graecia, Catanzaro, Italy G Annesi: Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy A Quattrone : Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy - Institute of Neurology, Department of Medical Sciences, University Magna Graecia, Catanzaro, Italy (literal)
Titolo
  • LRRK2 G6055A mutation in Italian patients with familial or sporadic Parkinson's disease (literal)
Abstract
  • Alterations in the leucine-rich kinase 2 gene (LRRK2; MIM *609007) have been shown to cause an autosomal dominant form of PARK8-linked parkinsonism (1, 2). Within this gene, the G6055A mutation (exon 41; Gly2019Ser) represents the most common mutation described to date both in familial and in sporadic forms of Parkinson’s disease (PD). (literal)
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