Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association found.
Identifieur interne : 001F60 ( Ncbi/Checkpoint ); précédent : 001F59; suivant : 001F61Variable number tandem repeat dopamine transporter gene polymorphism and Parkinson's disease: no association found.
Auteurs : G. Mercier [France] ; J C Turpin ; G. LucotteSource :
- Journal of neurology [ 0340-5354 ] ; 1999.
English descriptors
- KwdEn :
- Adult, Aged, Carrier Proteins (genetics), Dopamine Plasma Membrane Transport Proteins, Female, Genetic Markers, Humans, Male, Membrane Glycoproteins, Membrane Transport Proteins, Middle Aged, Minisatellite Repeats (genetics), Nerve Tissue Proteins, Parkinson Disease (blood), Parkinson Disease (genetics), Polymerase Chain Reaction, Polymorphism, Genetic (genetics).
- MESH :
- chemical , genetics : Carrier Proteins.
- blood : Parkinson Disease.
- genetics : Minisatellite Repeats, Parkinson Disease, Polymorphism, Genetic.
- Adult, Aged, Dopamine Plasma Membrane Transport Proteins, Female, Genetic Markers, Humans, Male, Membrane Glycoproteins, Membrane Transport Proteins, Middle Aged, Nerve Tissue Proteins, Polymerase Chain Reaction.
Abstract
We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson's disease in a French population. Five alleles were detected, consisting of 7, 8, 9, 10 and 11 copies of the 40-base pair repeat sequence, of which the 10-copy allele was the most common. There was no significant difference between the patients and the control subjects in the distribution frequencies of the alleles or genotypes, or in ages at onset in patients between the main allelic classes.
PubMed: 9987713
Affiliations:
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pubmed:9987713Le document en format XML
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<front><div type="abstract" xml:lang="en">We studied a variable number of tandem repeat polymorphisms in the dopamine transporter gene in search of an association with Parkinson's disease in a French population. Five alleles were detected, consisting of 7, 8, 9, 10 and 11 copies of the 40-base pair repeat sequence, of which the 10-copy allele was the most common. There was no significant difference between the patients and the control subjects in the distribution frequencies of the alleles or genotypes, or in ages at onset in patients between the main allelic classes.</div>
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