MovDisordV3, Main, Exploration, bibRecord, 000785

Screening for rare sequence variants in the THAP1 gene in a primary dystonia cohort.

Identifieur interne : 000785 ( Main/Exploration ); précédent : 000784; suivant : 000786

Screening for rare sequence variants in the THAP1 gene in a primary dystonia cohort.

Auteurs : Jeremy R B. Newman [Australie] ; Alexander C. Lehn ; Richard S. Boyle ; Peter A. Silburn ; George D. Mellick

Source :

Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2013.

RBID : pubmed:23649788

English descriptors

KwdEn :
- Apoptosis Regulatory Proteins (genetics), DNA-Binding Proteins (genetics), Dystonic Disorders (genetics), Genetic Testing, Genetic Variation, Humans, Nuclear Proteins (genetics), Pedigree.
MESH :
- chemical , genetics : Apoptosis Regulatory Proteins, DNA-Binding Proteins, Nuclear Proteins.
- genetics : Dystonic Disorders.
- Genetic Testing, Genetic Variation, Humans, Pedigree.

DOI: 10.1002/mds.25479
PubMed: 23649788

Affiliations:

Australie

Le document en format XML

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<author><name sortKey="Newman, Jeremy R B" sort="Newman, Jeremy R B" uniqKey="Newman J" first="Jeremy R B" last="Newman">Jeremy R B. Newman</name>
<affiliation wicri:level="1"><nlm:affiliation>Eskitis Institute for Cell and Molecular Therapies, Griffith University, Brisbane, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
<wicri:regionArea>Eskitis Institute for Cell and Molecular Therapies, Griffith University, Brisbane</wicri:regionArea>
<wicri:noRegion>Brisbane</wicri:noRegion>
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<author><name sortKey="Lehn, Alexander C" sort="Lehn, Alexander C" uniqKey="Lehn A" first="Alexander C" last="Lehn">Alexander C. Lehn</name>
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<author><name sortKey="Boyle, Richard S" sort="Boyle, Richard S" uniqKey="Boyle R" first="Richard S" last="Boyle">Richard S. Boyle</name>
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<author><name sortKey="Silburn, Peter A" sort="Silburn, Peter A" uniqKey="Silburn P" first="Peter A" last="Silburn">Peter A. Silburn</name>
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<author><name sortKey="Mellick, George D" sort="Mellick, George D" uniqKey="Mellick G" first="George D" last="Mellick">George D. Mellick</name>
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<author><name sortKey="Lehn, Alexander C" sort="Lehn, Alexander C" uniqKey="Lehn A" first="Alexander C" last="Lehn">Alexander C. Lehn</name>
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<author><name sortKey="Boyle, Richard S" sort="Boyle, Richard S" uniqKey="Boyle R" first="Richard S" last="Boyle">Richard S. Boyle</name>
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<author><name sortKey="Silburn, Peter A" sort="Silburn, Peter A" uniqKey="Silburn P" first="Peter A" last="Silburn">Peter A. Silburn</name>
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<series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title>
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<term>Genetic Variation</term>
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<term>Nuclear Proteins (genetics)</term>
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<name sortKey="Mellick, George D" sort="Mellick, George D" uniqKey="Mellick G" first="George D" last="Mellick">George D. Mellick</name>
<name sortKey="Silburn, Peter A" sort="Silburn, Peter A" uniqKey="Silburn P" first="Peter A" last="Silburn">Peter A. Silburn</name>
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Movement Disorders (revue)

Screening for rare sequence variants in the THAP1 gene in a primary dystonia cohort.

Screening for rare sequence variants in the THAP1 gene in a primary dystonia cohort.

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

Pour générer des pages wiki

	Movement Disorders (revue)
	Attention, ce site est en cours de développement ! Attention, site généré par des moyens informatiques à partir de corpus bruts. Les informations ne sont donc pas validées.