VPS35 Mutations in Parkinson Disease-Reference-Cited by-同舟云学术

VPS35 Mutations in Parkinson Disease

Published:2011-07 Issue:1 Volume:89 Page:162-167
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference24 articles.

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3. Genetics of Parkinson disease: Paradigm shifts and future prospects;Farrer;Nat. Rev. Genet.,2006

4. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: A meta-analysis of genome-wide association studies;Nalls;Lancet,2011

5. Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family;Wider;Parkinsonism Relat. Disord.,2008

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