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 : 000B76Frequencies 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 LeeSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2003.
English descriptors
- KwdEn :
- Alcohol Dehydrogenase (genetics), Alcohol Dehydrogenase (metabolism), Case-Control Studies, Female, Humans, Isoenzymes (genetics), Isoenzymes (metabolism), Male, Middle Aged, Multiple System Atrophy (genetics), Multiple System Atrophy (metabolism), Polymerase Chain Reaction, Polymorphism, Single Nucleotide.
- MESH :
- chemical , genetics : Alcohol Dehydrogenase, Isoenzymes.
- chemical , metabolism : Alcohol Dehydrogenase, Isoenzymes.
- genetics : Multiple System Atrophy.
- metabolism : Multiple System Atrophy.
- Case-Control Studies, Female, Humans, Male, Middle Aged, Polymerase Chain Reaction, Polymorphism, Single Nucleotide.
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:14502680Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls.</title>
<author><name sortKey="Kim, Hyun Sook" sort="Kim, Hyun Sook" uniqKey="Kim H" first="Hyun Sook" last="Kim">Hyun Sook Kim</name>
<affiliation wicri:level="3"><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>
<placeName><settlement type="city">Séoul</settlement>
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<author><name sortKey="Lee, Myung Sik" sort="Lee, Myung Sik" uniqKey="Lee M" first="Myung Sik" last="Lee">Myung Sik Lee</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">Frequencies of single nucleotide polymorphism in alcohol dehydrogenase7 gene in patients with multiple system atrophy and controls.</title>
<author><name sortKey="Kim, Hyun Sook" sort="Kim, Hyun Sook" uniqKey="Kim H" first="Hyun Sook" last="Kim">Hyun Sook Kim</name>
<affiliation wicri:level="3"><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>
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<placeName><settlement type="city">Séoul</settlement>
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<author><name sortKey="Lee, Myung Sik" sort="Lee, Myung Sik" uniqKey="Lee M" first="Myung Sik" last="Lee">Myung Sik Lee</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="ISSN">0885-3185</idno>
<imprint><date when="2003" type="published">2003</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><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>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Alcohol Dehydrogenase</term>
<term>Isoenzymes</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Alcohol Dehydrogenase</term>
<term>Isoenzymes</term>
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<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Multiple System Atrophy</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Multiple System Atrophy</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Case-Control Studies</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Polymerase Chain Reaction</term>
<term>Polymorphism, Single Nucleotide</term>
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<front><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>
</front>
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