The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.
Identifieur interne : 000B90 ( Main/Exploration ); précédent : 000B89; suivant : 000B91The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's disease.
Auteurs : Ilaria Guella ; Giulia Soldà ; Roberto Cilia ; Gianni Pezzoli ; Rosanna Asselta ; Stefano Duga ; Stefano GoldwurmSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Vesicular Transport Proteins.
- genetics : Parkinson Disease.
- Adult, Aged, Aged, 80 and over, Female, Genetic Association Studies, Humans, Male, Middle Aged, Mutation, Polymorphism, Single Nucleotide.
DOI: 10.1002/mds.24927
PubMed: 22278960
Affiliations:
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Le document en format XML
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Duga</name></author><author><name sortKey="Goldwurm, Stefano" sort="Goldwurm, Stefano" uniqKey="Goldwurm S" first="Stefano" last="Goldwurm">Stefano Goldwurm</name></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2012">2012</date><idno type="doi">10.1002/mds.24927</idno><idno type="RBID">pubmed:22278960</idno><idno type="pmid">22278960</idno><idno type="wicri:Area/PubMed/Corpus">000E88</idno><idno type="wicri:Area/PubMed/Curation">000E88</idno><idno type="wicri:Area/PubMed/Checkpoint">000C01</idno><idno type="wicri:Area/Ncbi/Merge">003542</idno><idno type="wicri:Area/Ncbi/Curation">003542</idno><idno type="wicri:Area/Ncbi/Checkpoint">003542</idno><idno type="wicri:Area/Main/Merge">000B94</idno><idno type="wicri:Area/Main/Curation">000B90</idno><idno type="wicri:Area/Main/Exploration">000B90</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">The Asp620asn mutation in VPS35 is not a common cause of familial Parkinson's 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Goldwurm</name></author></analytic><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></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Adult</term><term>Aged</term><term>Aged, 80 and over</term><term>Female</term><term>Genetic Association Studies</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Mutation</term><term>Parkinson Disease (genetics)</term><term>Polymorphism, Single Nucleotide</term><term>Vesicular Transport Proteins (genetics)</term></keywords><keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Vesicular Transport Proteins</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Parkinson Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Adult</term><term>Aged</term><term>Aged, 80 and over</term><term>Female</term><term>Genetic Association Studies</term><term>Humans</term><term>Male</term><term>Middle Aged</term><term>Mutation</term><term>Polymorphism, Single Nucleotide</term></keywords></textClass></profileDesc></teiHeader></TEI><affiliations><list></list><tree><noCountry><name sortKey="Asselta, Rosanna" sort="Asselta, Rosanna" uniqKey="Asselta R" first="Rosanna" last="Asselta">Rosanna Asselta</name><name sortKey="Cilia, Roberto" sort="Cilia, Roberto" uniqKey="Cilia R" first="Roberto" last="Cilia">Roberto Cilia</name><name sortKey="Duga, Stefano" sort="Duga, Stefano" uniqKey="Duga S" first="Stefano" last="Duga">Stefano Duga</name><name sortKey="Goldwurm, Stefano" sort="Goldwurm, Stefano" uniqKey="Goldwurm S" first="Stefano" last="Goldwurm">Stefano Goldwurm</name><name sortKey="Guella, Ilaria" sort="Guella, Ilaria" uniqKey="Guella I" first="Ilaria" last="Guella">Ilaria Guella</name><name sortKey="Pezzoli, Gianni" sort="Pezzoli, Gianni" uniqKey="Pezzoli G" first="Gianni" last="Pezzoli">Gianni Pezzoli</name><name sortKey="Solda, Giulia" sort="Solda, Giulia" uniqKey="Solda G" first="Giulia" last="Soldà">Giulia Soldà</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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