Your browser doesn't support javascript.
loading
VPS35 mutations in Parkinson disease.
Vilariño-Güell, Carles; Wider, Christian; Ross, Owen A; Dachsel, Justus C; Kachergus, Jennifer M; Lincoln, Sarah J; Soto-Ortolaza, Alexandra I; Cobb, Stephanie A; Wilhoite, Greggory J; Bacon, Justin A; Behrouz, Bahareh; Melrose, Heather L; Hentati, Emna; Puschmann, Andreas; Evans, Daniel M; Conibear, Elizabeth; Wasserman, Wyeth W; Aasly, Jan O; Burkhard, Pierre R; Djaldetti, Ruth; Ghika, Joseph; Hentati, Faycal; Krygowska-Wajs, Anna; Lynch, Tim; Melamed, Eldad; Rajput, Alex; Rajput, Ali H; Solida, Alessandra; Wu, Ruey-Meei; Uitti, Ryan J; Wszolek, Zbigniew K; Vingerhoets, François; Farrer, Matthew J.
Affiliation
  • Vilariño-Güell C; Department of Medical Genetics, University of British Columbia, Vancouver, Canada. carles@can.ubc.ca
Am J Hum Genet ; 89(1): 162-7, 2011 Jul 15.
Article in En | MEDLINE | ID: mdl-21763482
Subject(s)
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Vesicular Transport Proteins / Mutation Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2011 Type: Article Affiliation country: Canada
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Parkinson Disease / Vesicular Transport Proteins / Mutation Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Am J Hum Genet Year: 2011 Type: Article Affiliation country: Canada