DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. (Articolo in rivista)

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  • DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. (Articolo in rivista) (literal)
Anno
  • 2005-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/ana.20666 (literal)
Alternative label
  • Annesi G 1; Savettieri G 2; Pugliese P 3; D'Amelio M 2; Tarantino P 1; Ragonese P 2; La Bella V 2; Piccoli T 2; Civitelli D 1; Annesi F 1; Fierro B 2; Piccoli F 2; Arabia G 3; Caracciolo M 1; Ciro' Candiano IC 1; Quattrone A 1-3. (2005)
    DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex.
    in Annals of neurology
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Annesi G 1; Savettieri G 2; Pugliese P 3; D'Amelio M 2; Tarantino P 1; Ragonese P 2; La Bella V 2; Piccoli T 2; Civitelli D 1; Annesi F 1; Fierro B 2; Piccoli F 2; Arabia G 3; Caracciolo M 1; Ciro' Candiano IC 1; Quattrone A 1-3. (literal)
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  • 803 (literal)
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  • http://onlinelibrary.wiley.com/doi/10.1002/ana.20666/pdf (literal)
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  • 58 (literal)
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Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1 Institute of Neurological Sciences, National Research Council, Piano Lago di Mangone, Cosenza, Italy 2 Department of Neurology, Ophthalmology, Otorinolaringology and Psychiatry, University of Palermo, Palermo, Italy 3 Istitute of Neurology, University Magna Graecia, Catanzaro, Italy. (literal)
Titolo
  • DJ-1 mutations and parkinsonism-dementia-amyotrophic lateral sclerosis complex. (literal)
Abstract
  • DJ-1 gene mutations have been found to cause early-onset Parkinson's disease. We report a family from southern Italy with three brothers affected by early-onset parkinsonism, dementia, and amyotrophic lateral sclerosis. Molecular analysis of the DJ-1 gene in two living patients showed a novel homozygous mutation in exon 7 (E163K) and a new homozygous mutation (g.168_185dup) in the promoter region of the gene. Both mutations cosegregated with the disease and were detected in a heterozygous state in the patients' mother and their healthy siblings. Our findings expand the spectrum of clinical presentations associated with mutations in DJ-1 gene. (literal)
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