MovDisordV3, Main, Exploration, bibRecord, 003248

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early‐onset Parkinson's Disease

Identifieur interne : 003248 ( Main/Exploration ); précédent : 003247; suivant : 003249

Prevalence of the H1069Q mutation in ATP7B in discordant pairs with early‐onset Parkinson's Disease

Auteurs : Jens Carsten Möller [Allemagne] ; Barbara Leinweber [Allemagne] ; Ida Rissling [Allemagne] ; Wolfgang Herman Oertel [Allemagne] ; Oliver Bandmann [Royaume-Uni] ; Hartmut H. Schmidt [Allemagne]

Source :

Movement Disorders [ 0885-3185 ] ; 2006-10.

RBID : ISTEX:813091D169B9C23FF588A89A204457EE066AF41D

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.

Url:

https://api.istex.fr/document/813091D169B9C23FF588A89A204457EE066AF41D/fulltext/pdf

DOI: 10.1002/mds.21066

Affiliations:

Le document en format XML

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<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="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>
<affiliation wicri:level="1"><country xml:lang="fr">Royaume-Uni</country>
<wicri:regionArea>Division of Genomic Medicine, Academic Neurology Unit, University of Sheffield, Sheffield</wicri:regionArea>
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<author><name sortKey="Schmidt, Hartmut H" sort="Schmidt, Hartmut H" uniqKey="Schmidt H" first="Hartmut H." last="Schmidt">Hartmut H. Schmidt</name>
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<term>Alleles</term>
<term>Cation Transport Proteins (genetics)</term>
<term>Exons (genetics)</term>
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<term>Genotype</term>
<term>Hepatolenticular Degeneration (diagnosis)</term>
<term>Hepatolenticular Degeneration (genetics)</term>
<term>Humans</term>
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<term>Middle Aged</term>
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<term>Parkinson Disease (genetics)</term>
<term>Phenotype</term>
<term>Siblings</term>
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<term>Cation Transport Proteins</term>
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<term>Parkinson Disease</term>
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<term>Parkinson Disease</term>
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<term>Age Factors</term>
<term>Aged</term>
<term>Alleles</term>
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<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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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...)

Le document en format XML

Pour manipuler ce document sous Unix (Dilib)

Pour mettre un lien sur cette page dans le réseau Wicri

	Movement Disorders (revue)
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