DNAJC13 genetic variants in parkinsonism.
Identifieur interne : 000777 ( Main/Curation ); précédent : 000776; suivant : 000778DNAJC13 genetic variants in parkinsonism.
Auteurs : Emil K. Gustavsson [Norvège] ; Joanne Trinh ; Ilaria Guella ; Carles Vilari O-Güell ; Silke Appel-Cresswell ; A Jon Stoessl ; Joseph K. Tsui ; Martin Mckeown ; Alex Rajput ; Ali H. Rajput ; Jan O. Aasly ; Matthew J. FarrerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2015.
English descriptors
- KwdEn :
- Age of Onset, Female, Gene Frequency (genetics), Genetic Predisposition to Disease, Genotype, Humans, Male, Molecular Chaperones (genetics), Mutation, Missense (genetics), Parkinson Disease (diagnosis), Parkinson Disease (genetics), Parkinsonian Disorders (diagnosis), Parkinsonian Disorders (genetics).
- MESH :
- chemical , genetics : Molecular Chaperones.
- diagnosis : Parkinson Disease, Parkinsonian Disorders.
- genetics : Gene Frequency, Mutation, Missense, Parkinson Disease, Parkinsonian Disorders.
- Age of Onset, Female, Genetic Predisposition to Disease, Genotype, Humans, Male.
Abstract
A novel mutation (p.N855S) in DNAJC13 has been linked to familial, late-onset Lewy body parkinsonism in a Dutch-German-Russian Mennonite multi-incident kindred.
DOI: 10.1002/mds.26064
PubMed: 25393719
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pubmed:25393719Le document en format XML
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<front><div type="abstract" xml:lang="en">A novel mutation (p.N855S) in DNAJC13 has been linked to familial, late-onset Lewy body parkinsonism in a Dutch-German-Russian Mennonite multi-incident kindred.</div>
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