DNAJC13 mutations in Parkinson disease.

Vilariño-Güell, Carles; Rajput, Alex; Milnerwood, Austen J; Shah, Brinda; Szu-Tu, Chelsea; Trinh, Joanne; Yu, Irene; Encarnacion, Mary; Munsie, Lise N; Tapia, Lucia; Gustavsson, Emil K; Chou, Patrick; Tatarnikov, Igor; Evans, Daniel M; Pishotta, Frederick T; Volta, Mattia; Beccano-Kelly, Dayne; Thompson, Christina; Lin, Michelle K; Sherman, Holly E; Han, Heather J; Guenther, Bruce L; Wasserman, Wyeth W; Bernard, Virginie; Ross, Colin J; Appel-Cresswell, Silke; Stoessl, A Jon; Robinson, Christopher A; Dickson, Dennis W; Ross, Owen A; Wszolek, Zbigniew K; Aasly, Jan O; Wu, Ruey-Meei; Hentati, Faycal; Gibson, Rachel A; McPherson, Peter S; Girard, Martine; Rajput, Michele; Rajput, Ali H; Farrer, Matthew J

Vilariño-Güell, Carles; Rajput, Alex; Milnerwood, Austen J; Shah, Brinda; Szu-Tu, Chelsea; Trinh, Joanne; Yu, Irene; Encarnacion, Mary; Munsie, Lise N; Tapia, Lucia; Gustavsson, Emil K; Chou, Patrick; Tatarnikov, Igor; Evans, Daniel M; Pishotta, Frederick T; Volta, Mattia; Beccano-Kelly, Dayne; Thompson, Christina; Lin, Michelle K; Sherman, Holly E; Han, Heather J; Guenther, Bruce L; Wasserman, Wyeth W; Bernard, Virginie; Ross, Colin J; Appel-Cresswell, Silke; Stoessl, A Jon; Robinson, Christopher A; Dickson, Dennis W; Ross, Owen A; Wszolek, Zbigniew K; Aasly, Jan O; Wu, Ruey-Meei; Hentati, Faycal; Gibson, Rachel A; McPherson, Peter S; Girard, Martine; Rajput, Michele; Rajput, Ali H; Farrer, Matthew J.

Affiliation

Vilariño-Güell C; Department of Medical Genetics, University of British Columbia, Vancouver, BC V6T 2B5, Canada.

Hum Mol Genet ; 23(7): 1794-801, 2014 Apr 01.

Article in En | MEDLINE | ID: mdl-24218364

Subject(s)

Lewy Bodies/genetics; Molecular Chaperones/genetics; Mutation/genetics; Parkinson Disease/genetics; Adult; Age of Onset; Aged; Base Sequence; Case-Control Studies; Cells, Cultured; Endocytosis/genetics; Endosomes/genetics; Family; Female; Genetic Predisposition to Disease; Haplotypes; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Lewy Body Disease/genetics; Male; Middle Aged; Molecular Chaperones/immunology; Pedigree; Protein Serine-Threonine Kinases/genetics; Sequence Alignment; Sequence Analysis, DNA; Vesicular Transport Proteins/genetics

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google

Full text: 1 Database: MEDLINE Main subject: Parkinson Disease / Lewy Bodies / Molecular Chaperones / Mutation Type of study: Observational_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2014 Type: Article Affiliation country: Canada

Fulltext

Add to My VHL

XML

PubMed Links

Search on Google