The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
Identifieur interne : 001828 ( Ncbi/Merge ); précédent : 001827; suivant : 001829The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.
Auteurs : Ina Schmitt ; Ullrich Wüllner ; Daniel G. Healy ; Nicholas W. Wood ; Heike Kölsch ; Reinhard HeunSource :
- Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2006.
Descripteurs français
- Wicri :
- geographic : Allemagne.
English descriptors
- KwdEn :
- Alcohol Dehydrogenase (genetics), Case-Control Studies, Codon, Terminator (genetics), DNA Mutational Analysis, Female, Gene Frequency, Genetics, Population, Germany (epidemiology), Germany (ethnology), Glycine (genetics), Great Britain (epidemiology), Great Britain (ethnology), Heterozygote, Humans, Male, Multiple System Atrophy (genetics), Mutation.
- MESH :
- chemical , genetics : Alcohol Dehydrogenase, Codon, Terminator, Glycine.
- geographic , epidemiology : Germany, Great Britain.
- geographic , ethnology : Germany, Great Britain.
- genetics : Multiple System Atrophy.
- Case-Control Studies, DNA Mutational Analysis, Female, Gene Frequency, Genetics, Population, Heterozygote, Humans, Male, Mutation.
DOI: 10.1002/mds.21082
PubMed: 16960859
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: 002B11
- to stream PubMed, to step Curation: 002B11
- to stream PubMed, to step Checkpoint: 002A57
Links to Exploration step
pubmed:16960859Le document en format XML
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<author><name sortKey="Schmitt, Ina" sort="Schmitt, Ina" uniqKey="Schmitt I" first="Ina" last="Schmitt">Ina Schmitt</name>
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<author><name sortKey="Wullner, Ullrich" sort="Wullner, Ullrich" uniqKey="Wullner U" first="Ullrich" last="Wüllner">Ullrich Wüllner</name>
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<author><name sortKey="Healy, Daniel G" sort="Healy, Daniel G" uniqKey="Healy D" first="Daniel G" last="Healy">Daniel G. Healy</name>
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<author><name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W" last="Wood">Nicholas W. Wood</name>
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<author><name sortKey="Kolsch, Heike" sort="Kolsch, Heike" uniqKey="Kolsch H" first="Heike" last="Kölsch">Heike Kölsch</name>
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<author><name sortKey="Heun, Reinhard" sort="Heun, Reinhard" uniqKey="Heun R" first="Reinhard" last="Heun">Reinhard Heun</name>
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<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetics, Population</term>
<term>Germany (epidemiology)</term>
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<term>Glycine (genetics)</term>
<term>Great Britain (epidemiology)</term>
<term>Great Britain (ethnology)</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Multiple System Atrophy (genetics)</term>
<term>Mutation</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Alcohol Dehydrogenase</term>
<term>Codon, Terminator</term>
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<term>DNA Mutational Analysis</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetics, Population</term>
<term>Heterozygote</term>
<term>Humans</term>
<term>Male</term>
<term>Mutation</term>
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<keywords scheme="Wicri" type="geographic" xml:lang="fr"><term>Allemagne</term>
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<DateCreated><Year>2006</Year>
<Month>12</Month>
<Day>05</Day>
</DateCreated>
<DateCompleted><Year>2007</Year>
<Month>02</Month>
<Day>20</Day>
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<DateRevised><Year>2013</Year>
<Month>11</Month>
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<JournalIssue CitedMedium="Print"><Volume>21</Volume>
<Issue>11</Issue>
<PubDate><Year>2006</Year>
<Month>Nov</Month>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>The ADH1C stop mutation in multiple system atrophy patients and healthy probands in the United Kingdom and Germany.</ArticleTitle>
<Pagination><MedlinePgn>2034</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Schmitt</LastName>
<ForeName>Ina</ForeName>
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<Author ValidYN="Y"><LastName>Wüllner</LastName>
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<Author ValidYN="Y"><LastName>Healy</LastName>
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<Language>eng</Language>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D004252">DNA Mutational Analysis</DescriptorName>
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<MeshHeading><DescriptorName MajorTopicYN="N" UI="D005787">Gene Frequency</DescriptorName>
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<QualifierName MajorTopicYN="N" UI="Q000208">ethnology</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006579">Heterozygote</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D006801">Humans</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D008297">Male</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D019578">Multiple System Atrophy</DescriptorName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="Y" UI="D009154">Mutation</DescriptorName>
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<affiliations><list></list>
<tree><noCountry><name sortKey="Healy, Daniel G" sort="Healy, Daniel G" uniqKey="Healy D" first="Daniel G" last="Healy">Daniel G. Healy</name>
<name sortKey="Heun, Reinhard" sort="Heun, Reinhard" uniqKey="Heun R" first="Reinhard" last="Heun">Reinhard Heun</name>
<name sortKey="Kolsch, Heike" sort="Kolsch, Heike" uniqKey="Kolsch H" first="Heike" last="Kölsch">Heike Kölsch</name>
<name sortKey="Schmitt, Ina" sort="Schmitt, Ina" uniqKey="Schmitt I" first="Ina" last="Schmitt">Ina Schmitt</name>
<name sortKey="Wood, Nicholas W" sort="Wood, Nicholas W" uniqKey="Wood N" first="Nicholas W" last="Wood">Nicholas W. Wood</name>
<name sortKey="Wullner, Ullrich" sort="Wullner, Ullrich" uniqKey="Wullner U" first="Ullrich" last="Wüllner">Ullrich Wüllner</name>
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