MovDisordV3, PubMed, Checkpoint, bibRecord, 002B48

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease.

Identifieur interne : 002B48 ( PubMed/Checkpoint ); précédent : 002B47; suivant : 002B49

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease.

Auteurs : Jens Carsten Möller ; Barbara Leinweber ; Ida Rissling ; Wolfgang Herman Oertel ; Oliver Bandmann ; Hartmut H-J Schmidt

Source :

Movement disorders : official journal of the Movement Disorder Society [ 0885-3185 ] ; 2006.

RBID : pubmed:16941464

English descriptors

KwdEn :
- Adenosine Triphosphatases (genetics), Adult, Age Factors, Aged, Alleles, Cation Transport Proteins (genetics), Exons (genetics), Female, Genotype, Hepatolenticular Degeneration (diagnosis), Hepatolenticular Degeneration (genetics), Humans, Male, Middle Aged, Mutation (genetics), Parkinson Disease (diagnosis), Parkinson Disease (genetics), Phenotype, Siblings.
MESH :
- chemical , genetics : Adenosine Triphosphatases, Cation Transport Proteins.
- diagnosis : Hepatolenticular Degeneration, Parkinson Disease.
- genetics : Exons, Hepatolenticular Degeneration, Mutation, Parkinson Disease.
- Adult, Age Factors, Aged, Alleles, Female, Genotype, Humans, Male, Middle Aged, Phenotype, Siblings.

DOI: 10.1002/mds.21066
PubMed: 16941464

Affiliations:

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pubmed:16941464

Le document en format XML

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<author><name sortKey="Moller, Jens Carsten" sort="Moller, Jens Carsten" uniqKey="Moller J" first="Jens Carsten" last="Möller">Jens Carsten Möller</name>
</author>
<author><name sortKey="Leinweber, Barbara" sort="Leinweber, Barbara" uniqKey="Leinweber B" first="Barbara" last="Leinweber">Barbara Leinweber</name>
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<author><name sortKey="Rissling, Ida" sort="Rissling, Ida" uniqKey="Rissling I" first="Ida" last="Rissling">Ida Rissling</name>
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<author><name sortKey="Oertel, Wolfgang Herman" sort="Oertel, Wolfgang Herman" uniqKey="Oertel W" first="Wolfgang Herman" last="Oertel">Wolfgang Herman Oertel</name>
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<author><name sortKey="Bandmann, Oliver" sort="Bandmann, Oliver" uniqKey="Bandmann O" first="Oliver" last="Bandmann">Oliver Bandmann</name>
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<author><name sortKey="Schmidt, Hartmut H J" sort="Schmidt, Hartmut H J" uniqKey="Schmidt H" first="Hartmut H-J" last="Schmidt">Hartmut H-J Schmidt</name>
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<term>Parkinson Disease</term>
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<keywords scheme="MESH" xml:lang="en"><term>Adult</term>
<term>Age Factors</term>
<term>Aged</term>
<term>Alleles</term>
<term>Female</term>
<term>Genotype</term>
<term>Humans</term>
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<term>Middle Aged</term>
<term>Phenotype</term>
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<Day>26</Day>
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<DateCompleted><Year>2007</Year>
<Month>02</Month>
<Day>02</Day>
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<Article PubModel="Print"><Journal><ISSN IssnType="Print">0885-3185</ISSN>
<JournalIssue CitedMedium="Print"><Volume>21</Volume>
<Issue>10</Issue>
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<Month>Oct</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>Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease.</ArticleTitle>
<Pagination><MedlinePgn>1789-90</MedlinePgn>
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<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Möller</LastName>
<ForeName>Jens Carsten</ForeName>
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<QualifierName MajorTopicYN="N" UI="Q000175">diagnosis</QualifierName>
<QualifierName MajorTopicYN="Y" UI="Q000235">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D010641">Phenotype</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName MajorTopicYN="N" UI="D035781">Siblings</DescriptorName>
</MeshHeading>
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<tree><noCountry><name sortKey="Bandmann, Oliver" sort="Bandmann, Oliver" uniqKey="Bandmann O" first="Oliver" last="Bandmann">Oliver Bandmann</name>
<name sortKey="Leinweber, Barbara" sort="Leinweber, Barbara" uniqKey="Leinweber B" first="Barbara" last="Leinweber">Barbara Leinweber</name>
<name sortKey="Moller, Jens Carsten" sort="Moller, Jens Carsten" uniqKey="Moller J" first="Jens Carsten" last="Möller">Jens Carsten Möller</name>
<name sortKey="Oertel, Wolfgang Herman" sort="Oertel, Wolfgang Herman" uniqKey="Oertel W" first="Wolfgang Herman" last="Oertel">Wolfgang Herman Oertel</name>
<name sortKey="Rissling, Ida" sort="Rissling, Ida" uniqKey="Rissling I" first="Ida" last="Rissling">Ida Rissling</name>
<name sortKey="Schmidt, Hartmut H J" sort="Schmidt, Hartmut H J" uniqKey="Schmidt H" first="Hartmut H-J" last="Schmidt">Hartmut H-J Schmidt</name>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease.

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early-onset Parkinson's disease.

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