MovDisordV3, PubMed, Curation, bibRecord, 000C02

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.

Identifieur interne : 000C02 ( PubMed/Curation ); précédent : 000C01; suivant : 000C03

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.

Auteurs : Brent L. Fogel ; Mochtar Pribadi ; Sarah Pi ; Susan L. Perlman ; Daniel H. Geschwind ; Giovanni Coppola

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.

RBID : pubmed:23080112

English descriptors

KwdEn :
- Aged, Amyotrophic Lateral Sclerosis (genetics), Female, Genetic Predisposition to Disease (genetics), Humans, Male, Middle Aged, Mutation (genetics), Proteins (genetics), Spinocerebellar Ataxias (diagnosis), Spinocerebellar Ataxias (genetics).
MESH :
- chemical , genetics : Proteins.
- diagnosis : Spinocerebellar Ataxias.
- genetics : Amyotrophic Lateral Sclerosis, Genetic Predisposition to Disease, Mutation, Spinocerebellar Ataxias.
- Aged, Female, Humans, Male, Middle Aged.

DOI: 10.1002/mds.25245
PubMed: 23080112

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Le document en format XML

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<author><name sortKey="Fogel, Brent L" sort="Fogel, Brent L" uniqKey="Fogel B" first="Brent L" last="Fogel">Brent L. Fogel</name>
</author>
<author><name sortKey="Pribadi, Mochtar" sort="Pribadi, Mochtar" uniqKey="Pribadi M" first="Mochtar" last="Pribadi">Mochtar Pribadi</name>
</author>
<author><name sortKey="Pi, Sarah" sort="Pi, Sarah" uniqKey="Pi S" first="Sarah" last="Pi">Sarah Pi</name>
</author>
<author><name sortKey="Perlman, Susan L" sort="Perlman, Susan L" uniqKey="Perlman S" first="Susan L" last="Perlman">Susan L. Perlman</name>
</author>
<author><name sortKey="Geschwind, Daniel H" sort="Geschwind, Daniel H" uniqKey="Geschwind D" first="Daniel H" last="Geschwind">Daniel H. Geschwind</name>
</author>
<author><name sortKey="Coppola, Giovanni" sort="Coppola, Giovanni" uniqKey="Coppola G" first="Giovanni" last="Coppola">Giovanni Coppola</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en">C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.</title>
<author><name sortKey="Fogel, Brent L" sort="Fogel, Brent L" uniqKey="Fogel B" first="Brent L" last="Fogel">Brent L. Fogel</name>
</author>
<author><name sortKey="Pribadi, Mochtar" sort="Pribadi, Mochtar" uniqKey="Pribadi M" first="Mochtar" last="Pribadi">Mochtar Pribadi</name>
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<author><name sortKey="Pi, Sarah" sort="Pi, Sarah" uniqKey="Pi S" first="Sarah" last="Pi">Sarah Pi</name>
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<author><name sortKey="Perlman, Susan L" sort="Perlman, Susan L" uniqKey="Perlman S" first="Susan L" last="Perlman">Susan L. Perlman</name>
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<author><name sortKey="Geschwind, Daniel H" sort="Geschwind, Daniel H" uniqKey="Geschwind D" first="Daniel H" last="Geschwind">Daniel H. Geschwind</name>
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<author><name sortKey="Coppola, Giovanni" sort="Coppola, Giovanni" uniqKey="Coppola G" first="Giovanni" last="Coppola">Giovanni Coppola</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
<idno type="eISSN">1531-8257</idno>
<imprint><date when="2012" type="published">2012</date>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term>
<term>Amyotrophic Lateral Sclerosis (genetics)</term>
<term>Female</term>
<term>Genetic Predisposition to Disease (genetics)</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
<term>Mutation (genetics)</term>
<term>Proteins (genetics)</term>
<term>Spinocerebellar Ataxias (diagnosis)</term>
<term>Spinocerebellar Ataxias (genetics)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="diagnosis" xml:lang="en"><term>Spinocerebellar Ataxias</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Amyotrophic Lateral Sclerosis</term>
<term>Genetic Predisposition to Disease</term>
<term>Mutation</term>
<term>Spinocerebellar Ataxias</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Aged</term>
<term>Female</term>
<term>Humans</term>
<term>Male</term>
<term>Middle Aged</term>
</keywords>
</textClass>
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<DateCreated><Year>2013</Year>
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<Day>03</Day>
</DateCreated>
<DateCompleted><Year>2013</Year>
<Month>08</Month>
<Day>07</Day>
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<DateRevised><Year>2014</Year>
<Month>11</Month>
<Day>05</Day>
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<Issue>14</Issue>
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<Title>Movement disorders : official journal of the Movement Disorder Society</Title>
<ISOAbbreviation>Mov. Disord.</ISOAbbreviation>
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<ArticleTitle>C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.</ArticleTitle>
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<GrantList CompleteYN="Y"><Grant><GrantID>5T32NS048004-07</GrantID>
<Acronym>NS</Acronym>
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<Country>United States</Country>
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<Grant><GrantID>K08 MH086297</GrantID>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Neuron. 2011 Oct 20;72(2):245-56</RefSource>
<PMID Version="1">21944778</PMID>
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<CommentsCorrections RefType="Cites"><RefSource>Neuron. 2011 Oct 20;72(2):257-68</RefSource>
<PMID Version="1">21944779</PMID>
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<CommentsCorrections RefType="Cites"><RefSource>Brain. 2012 Mar;135(Pt 3):723-35</RefSource>
<PMID Version="1">22300876</PMID>
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<CommentsCorrections RefType="Cites"><RefSource>Clin Genet. 2013 Mar;83(3):279-83</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Lancet Neurol. 2012 Apr;11(4):323-30</RefSource>
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	Movement Disorders (revue)
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Movement Disorders (revue)

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.

C9ORF72 expansion is not a significant cause of sporadic spinocerebellar ataxia.

Source :

English descriptors

Links toward previous steps (curation, corpus...)

Links to Exploration step

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

Pour générer des pages wiki