Genetics of Parkinson's disease and parkinsonism
Identifieur interne : 001291 ( Main/Exploration ); précédent : 001290; suivant : 001292Genetics of Parkinson's disease and parkinsonism
Auteurs : John Hardy [États-Unis] ; Huaiban Cai [États-Unis] ; Mark R. Cookson [États-Unis] ; Katrina Gwinn-Hardy [États-Unis] ; Andrew Singleton [États-Unis]Source :
- Annals of Neurology [ 0364-5134 ] ; 2006-10.
Abstract
Until 10 years ago, conventional wisdom held that Parkinson's disease was not a genetic disorder. Since that time, there have been a plethora of genetic findings, culminating in the cloning of several genes that derive from the loci given the nomenclature PARK1‐PARK12 (OMIM 168600). Recently, these research findings have begun to impact clinical practice, and this impact is likely to increase. The primary purpose of this article is to outline these genetic advances, discuss their importance for current practice in clinical and related settings, and outline briefly how they are influencing research into the causes of and possible future treatments for this prevalent disorder. Ann Neurol 2006;60:389–398
Url:
DOI: 10.1002/ana.21022
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Cookson</name></author><author><name sortKey="Gwinn Ardy, Katrina" sort="Gwinn Ardy, Katrina" uniqKey="Gwinn Ardy K" first="Katrina" last="Gwinn-Hardy">Katrina Gwinn-Hardy</name></author><author><name sortKey="Singleton, Andrew" sort="Singleton, Andrew" uniqKey="Singleton A" first="Andrew" last="Singleton">Andrew Singleton</name></author></titleStmt><publicationStmt><idno type="wicri:source">ISTEX</idno><idno type="RBID">ISTEX:6FDB66D127E121559A4DA0D9AB3ACBE00279F873</idno><date when="2006" year="2006">2006</date><idno type="doi">10.1002/ana.21022</idno><idno type="url">https://api.istex.fr/document/6FDB66D127E121559A4DA0D9AB3ACBE00279F873/fulltext/pdf</idno><idno type="wicri:Area/Main/Corpus">001D61</idno><idno type="wicri:Area/Main/Curation">001A81</idno><idno type="wicri:Area/Main/Exploration">001291</idno></publicationStmt><sourceDesc><biblStruct><analytic><title level="a" type="main" xml:lang="en">Genetics of Parkinson's disease and parkinsonism</title><author><name sortKey="Hardy, John" sort="Hardy, John" uniqKey="Hardy J" first="John" last="Hardy">John Hardy</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">Maryland</region></placeName><wicri:cityArea>Laboratory of Neurogenetics, National Institute on Aging, National Institutes on Health, Bethesda</wicri:cityArea></affiliation></author><author><name sortKey="Cai, Huaiban" sort="Cai, Huaiban" uniqKey="Cai H" first="Huaiban" last="Cai">Huaiban Cai</name><affiliation wicri:level="2"><country xml:lang="fr">États-Unis</country><placeName><region type="state">Maryland</region></placeName><wicri:cityArea>Laboratory of Neurogenetics, National Institute on Aging, National Institutes on Health, Bethesda</wicri:cityArea></affiliation></author><author><name sortKey="Cookson, Mark R" sort="Cookson, Mark R" uniqKey="Cookson M" first="Mark R." last="Cookson">Mark R. 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Since that time, there have been a plethora of genetic findings, culminating in the cloning of several genes that derive from the loci given the nomenclature PARK1‐PARK12 (OMIM 168600). Recently, these research findings have begun to impact clinical practice, and this impact is likely to increase. The primary purpose of this article is to outline these genetic advances, discuss their importance for current practice in clinical and related settings, and outline briefly how they are influencing research into the causes of and possible future treatments for this prevalent disorder. 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