Double homozygous mutations (R275W and M432V) in the ParkinGene associated with late-onset Parkinson's disease.
Identifieur interne : 000378 ( Main/Exploration ); précédent : 000377; suivant : 000379Double homozygous mutations (R275W and M432V) in the ParkinGene associated with late-onset Parkinson's disease.
Auteurs : Jonathan Carr [Afrique du Sud] ; Ilaria Guella [Canada] ; Chelsea Szu-Tu [Canada] ; Sihaam Boolay [Afrique du Sud] ; Brigitte Glanzmann [Afrique du Sud] ; Matthew J. Farrer [Canada] ; Soraya Bardien [Afrique du Sud]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2016.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Ubiquitin-Protein Ligases.
- genetics : Late Onset Disorders, Mutation, Parkinson Disease.
- Aged, Female, Genetic Predisposition to Disease, Homozygote, Humans, Male, Middle Aged, Pedigree.
DOI: 10.1002/mds.26524
PubMed: 26860075
Affiliations:
Links toward previous steps (curation, corpus...)
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Le document en format XML
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<author><name sortKey="Szu Tu, Chelsea" sort="Szu Tu, Chelsea" uniqKey="Szu Tu C" first="Chelsea" last="Szu-Tu">Chelsea Szu-Tu</name>
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<term>Late Onset Disorders (genetics)</term>
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