Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy.

Di Maria, E; Tabaton, M; Vigo, T; Abbruzzese, G; Bellone, E; Donati, C; Frasson, E; Marchese, R; Montagna, P; Munoz, D G; Pramstaller, P P; Zanusso, G; Ajmar, F; Mandich, P

Di Maria, E; Tabaton, M; Vigo, T; Abbruzzese, G; Bellone, E; Donati, C; Frasson, E; Marchese, R; Montagna, P; Munoz, D G; Pramstaller, P P; Zanusso, G; Ajmar, F; Mandich, P.

Affiliation

Di Maria E; Department of Oncology, Biology and Genetics, University of Genova, Italy.

Ann Neurol ; 47(3): 374-7, 2000 Mar.

Article in En | MEDLINE | ID: mdl-10716259

Subject(s)

Basal Ganglia Diseases/genetics; Neurodegenerative Diseases/genetics; Supranuclear Palsy, Progressive/genetics; Aged; Alleles; Genotype; Haplotypes; Humans; Middle Aged; Polymorphism, Genetic/genetics

Search on Google

Add to My VHL

XML

PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Basal Ganglia Diseases / Supranuclear Palsy, Progressive / Neurodegenerative Diseases Limits: Aged / Humans / Middle aged Language: En Journal: Ann Neurol Year: 2000 Document type: Article Affiliation country: Italy Country of publication: United States

Search on Google

Add to My VHL

XML

PubMed Links