Movement Disorders (revue)

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Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls.

Identifieur interne : 000B75 ( Ncbi/Curation ); précédent : 000B74; suivant : 000B76

Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls.

Auteurs : Hyun Sook Kim [Corée du Sud] ; Myung Sik Lee

Source :

RBID : pubmed:14502680

English descriptors

Abstract

A polymerase chain reaction and direct sequencing of the ADH7 gene were carried out in 50 controls and 50 patients with probable multiple system atrophy (MSA). Seven SNPs, one insertion, and one mismatch were found in patients with MSA and controls. There was no significant difference in the frequencies of each SNP between the patients and the controls (P > 0.05). Interpretation of this negative finding should be cautious in view of the relatively small number of cases.

DOI: 10.1002/mds.10500
PubMed: 14502680

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pubmed:14502680

Le document en format XML

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<nlm:affiliation>Department of Neurology, Yongdong Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.</nlm:affiliation>
<country xml:lang="fr">Corée du Sud</country>
<wicri:regionArea>Department of Neurology, Yongdong Severance Hospital, Yonsei University College of Medicine, Seoul</wicri:regionArea>
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<title xml:lang="en">Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls.</title>
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<nlm:affiliation>Department of Neurology, Yongdong Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.</nlm:affiliation>
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<title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Alcohol Dehydrogenase (genetics)</term>
<term>Alcohol Dehydrogenase (metabolism)</term>
<term>Case-Control Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Isoenzymes (genetics)</term>
<term>Isoenzymes (metabolism)</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (genetics)</term>
<term>Multiple System Atrophy (metabolism)</term>
<term>Polymerase Chain Reaction</term>
<term>Polymorphism, Single Nucleotide</term>
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<term>Alcohol Dehydrogenase</term>
<term>Isoenzymes</term>
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<term>Alcohol Dehydrogenase</term>
<term>Isoenzymes</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Multiple System Atrophy</term>
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<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Multiple System Atrophy</term>
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<term>Case-Control Studies</term>
<term>Female</term>
<term>Humans</term>
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<div type="abstract" xml:lang="en">A polymerase chain reaction and direct sequencing of the ADH7 gene were carried out in 50 controls and 50 patients with probable multiple system atrophy (MSA). Seven SNPs, one insertion, and one mismatch were found in patients with MSA and controls. There was no significant difference in the frequencies of each SNP between the patients and the controls (P > 0.05). Interpretation of this negative finding should be cautious in view of the relatively small number of cases.</div>
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