Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?
Identifieur interne : 000264 ( PubMed/Curation ); précédent : 000263; suivant : 000265Polymorphism of NACP-Rep1 in Parkinson's disease: an etiologic link with essential tremor?
Auteurs : E Tan [États-Unis] ; T. Matsuura ; S. Nagamitsu ; M. Khajavi ; J. Jankovic ; T. AshizawaSource :
- Neurology [ 0028-3878 ] ; 2000.
English descriptors
- KwdEn :
- Adult, Age of Onset, Aged, Aged, 80 and over, Alleles, Essential Tremor (complications), Essential Tremor (genetics), Female, Genotype, Humans, Male, Middle Aged, Nerve Tissue Proteins (genetics), Parkinson Disease (complications), Parkinson Disease (genetics), Polymorphism, Genetic (genetics), Synucleins.
- MESH :
- chemical , genetics : Nerve Tissue Proteins.
- complications : Essential Tremor, Parkinson Disease.
- genetics : Essential Tremor, Parkinson Disease, Polymorphism, Genetic.
- Adult, Age of Onset, Aged, Aged, 80 and over, Alleles, Female, Genotype, Humans, Male, Middle Aged, Synucleins.
Abstract
An allele (263bp) of the nonamyloid component of plaques (NACP)-Repl polymorphism has shown association with sporadic PD in a German population. The authors studied this polymorphism in 100 American PD patients and 100 healthy controls. The authors also studied 46 essential tremor (ET) and 55 Huntington's disease (HD) patients. Allele 263bp was significantly higher in PD patients (OR = 3.86) and ET patients (OR = 6.42) but not HD patients, compared with healthy controls. The association of allele 263bp with PD and ET suggests a possible etiologic link between these two conditions.
PubMed: 10720300
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pubmed:10720300Le document en format XML
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<author><name sortKey="Tan, E K" sort="Tan, E K" uniqKey="Tan E" first="E" last="Tan">E Tan</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Baylor College of Medicine, Houston 77030, USA.</nlm:affiliation>
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<wicri:regionArea>Department of Neurology, Baylor College of Medicine, Houston 77030</wicri:regionArea>
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<author><name sortKey="Jankovic, J" sort="Jankovic, J" uniqKey="Jankovic J" first="J" last="Jankovic">J. Jankovic</name>
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<author><name sortKey="Ashizawa, T" sort="Ashizawa, T" uniqKey="Ashizawa T" first="T" last="Ashizawa">T. Ashizawa</name>
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<front><div type="abstract" xml:lang="en">An allele (263bp) of the nonamyloid component of plaques (NACP)-Repl polymorphism has shown association with sporadic PD in a German population. The authors studied this polymorphism in 100 American PD patients and 100 healthy controls. The authors also studied 46 essential tremor (ET) and 55 Huntington's disease (HD) patients. Allele 263bp was significantly higher in PD patients (OR = 3.86) and ET patients (OR = 6.42) but not HD patients, compared with healthy controls. The association of allele 263bp with PD and ET suggests a possible etiologic link between these two conditions.</div>
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<Abstract><AbstractText>An allele (263bp) of the nonamyloid component of plaques (NACP)-Repl polymorphism has shown association with sporadic PD in a German population. The authors studied this polymorphism in 100 American PD patients and 100 healthy controls. The authors also studied 46 essential tremor (ET) and 55 Huntington's disease (HD) patients. Allele 263bp was significantly higher in PD patients (OR = 3.86) and ET patients (OR = 6.42) but not HD patients, compared with healthy controls. The association of allele 263bp with PD and ET suggests a possible etiologic link between these two conditions.</AbstractText>
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