MovDisordV3, PubMed, Corpus, bibRecord, 000A88

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

Identifieur interne : 000A88 ( PubMed/Corpus ); précédent : 000A87; suivant : 000A89

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

Auteurs : Ignacio F. Mata ; Victoria Alvarez ; Renee Ribacoba ; Jon Infante ; María Sierra ; Pilar G Mez-Garre ; Pablo Mir ; Sarah Waldherr ; Dora Yearout ; Cyrus P. Zabetian

Source :

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

RBID : pubmed:23389884

English descriptors

KwdEn :
- Gene Frequency, Genetic Predisposition to Disease, Genotype, Haplotypes, Humans, Mutation, Missense (genetics), Parkinson Disease (epidemiology), Parkinson Disease (genetics), Protein-Serine-Threonine Kinases (genetics), South America (epidemiology), Spain (epidemiology).
MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- geographic , epidemiology : South America, Spain.
- epidemiology : Parkinson Disease.
- genetics : Mutation, Missense, Parkinson Disease.
- Gene Frequency, Genetic Predisposition to Disease, Genotype, Haplotypes, Humans.

DOI: 10.1002/mds.25293
PubMed: 23389884

Links to Exploration step

pubmed:23389884

Le document en format XML

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<author><name sortKey="Mata, Ignacio F" sort="Mata, Ignacio F" uniqKey="Mata I" first="Ignacio F" last="Mata">Ignacio F. Mata</name>
</author>
<author><name sortKey="Alvarez, Victoria" sort="Alvarez, Victoria" uniqKey="Alvarez V" first="Victoria" last="Alvarez">Victoria Alvarez</name>
</author>
<author><name sortKey="Ribacoba, Renee" sort="Ribacoba, Renee" uniqKey="Ribacoba R" first="Renee" last="Ribacoba">Renee Ribacoba</name>
</author>
<author><name sortKey="Infante, Jon" sort="Infante, Jon" uniqKey="Infante J" first="Jon" last="Infante">Jon Infante</name>
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<author><name sortKey="Sierra, Maria" sort="Sierra, Maria" uniqKey="Sierra M" first="María" last="Sierra">María Sierra</name>
</author>
<author><name sortKey="G Mez Garre, Pilar" sort="G Mez Garre, Pilar" uniqKey="G Mez Garre P" first="Pilar" last="G Mez-Garre">Pilar G Mez-Garre</name>
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<author><name sortKey="Mir, Pablo" sort="Mir, Pablo" uniqKey="Mir P" first="Pablo" last="Mir">Pablo Mir</name>
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<author><name sortKey="Waldherr, Sarah" sort="Waldherr, Sarah" uniqKey="Waldherr S" first="Sarah" last="Waldherr">Sarah Waldherr</name>
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<author><name sortKey="Yearout, Dora" sort="Yearout, Dora" uniqKey="Yearout D" first="Dora" last="Yearout">Dora Yearout</name>
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<author><name sortKey="Zabetian, Cyrus P" sort="Zabetian, Cyrus P" uniqKey="Zabetian C" first="Cyrus P" last="Zabetian">Cyrus P. Zabetian</name>
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<author><name sortKey="G Mez Garre, Pilar" sort="G Mez Garre, Pilar" uniqKey="G Mez Garre P" first="Pilar" last="G Mez-Garre">Pilar G Mez-Garre</name>
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<author><name sortKey="Zabetian, Cyrus P" sort="Zabetian, Cyrus P" uniqKey="Zabetian C" first="Cyrus P" last="Zabetian">Cyrus P. Zabetian</name>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Gene Frequency</term>
<term>Genetic Predisposition to Disease</term>
<term>Genotype</term>
<term>Haplotypes</term>
<term>Humans</term>
<term>Mutation, Missense (genetics)</term>
<term>Parkinson Disease (epidemiology)</term>
<term>Parkinson Disease (genetics)</term>
<term>Protein-Serine-Threonine Kinases (genetics)</term>
<term>South America (epidemiology)</term>
<term>Spain (epidemiology)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Protein-Serine-Threonine Kinases</term>
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<keywords scheme="MESH" type="geographic" qualifier="epidemiology" xml:lang="en"><term>South America</term>
<term>Spain</term>
</keywords>
<keywords scheme="MESH" qualifier="epidemiology" xml:lang="en"><term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Mutation, Missense</term>
<term>Parkinson Disease</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Gene Frequency</term>
<term>Genetic Predisposition to Disease</term>
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<term>Haplotypes</term>
<term>Humans</term>
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<ArticleTitle>Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.</ArticleTitle>
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<Author ValidYN="Y"><LastName>Zabetian</LastName>
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<CommentsCorrectionsList><CommentsCorrections RefType="Cites"><RefSource>Parkinsonism Relat Disord. 2007 Dec;13(8):509-15</RefSource>
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<CommentsCorrections RefType="Cites"><RefSource>Mov Disord. 2012 Jan;27(1):146-51</RefSource>
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	Movement Disorders (revue)
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Movement Disorders (revue)

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

Novel Lrrk2-p.S1761R mutation is not a common cause of Parkinson's disease in Spain.

Source :

English descriptors

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