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A frequent LRRK2 gene mutation associated with autosomal dominant Parkonson's disease

Italian Parkinson Genetics Network
2005-01-01
2005
The Neurology category covers resources concerned with the central and peripheral nervous system including the brain, spinal cord, nerves, and fluids. Coverage includes general and clinical neurology including neurosurgery, neuropsychiatry, neuropsychology, neurophysiology, neuroradiology, neuropediatrics, neuropathology, and neurobiology. Resources on cerebrovascular diseases, movement and spinal disorders, pain, dementia, headache, aphasiology, brain injury, paraplegia, stroke, and acupuncture are also included.
THE LANCET
WOS:000226610900028
2-s2.0-19944431081
Sì, ma tipo non specificato
Inglese
Internazionale
ELETTRONICO
365
9457
412
415
4
15680456
Tematica Ex SIR: Malattie neurodegenerative, aging brain e demenze. (Classif. Ex SIR:Articoli su riviste ISI )
LRRK2 GENE MUTATION; AUTOSOMAL DOMINANT; PARKONSON'S DISEASE
18
info:eu-repo/semantics/article
262
Di Fonzo, A; Rohé, Cf; Ferreira, J; Chien, Hf; Vacca, L; Stocchi, F; Guedes, L; Fabrizio, E; Manfredi, M; Vanacore, N; Goldwurm, S; Breedveld, G; Samp...espandi
1 Contributo su Rivista::1.1 Articolo in rivista
none
1.1 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/25901
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