Novel LRRK2 mutations in Parkinsonism.
Identifieur interne : 000434 ( PubMed/Corpus ); précédent : 000433; suivant : 000435Novel LRRK2 mutations in Parkinsonism.
Auteurs : Joanne Trinh ; Ilaria Guella ; Marna Mckenzie ; Emil K. Gustavsson ; Chelsea Szu-Tu ; Maria Skaalum Petersen ; Alex Rajput ; Ali H. Rajput ; Martin Mckeown ; Beom S. Jeon ; Jan O. Aasly ; Soraya Bardien ; Matthew J. FarrerSource :
- Parkinsonism & related disorders [ 1873-5126 ] ; 2015.
English descriptors
- KwdEn :
- Adult, Aged, Aged, 80 and over, Cross-Cultural Comparison, DNA Mutational Analysis, Exons (genetics), Female, Genetic Predisposition to Disease (genetics), Genotype, Humans, Leucine-Rich Repeat Serine-Threonine Protein Kinase-2, Male, Middle Aged, Mutation (genetics), Parkinsonian Disorders (genetics), Protein-Serine-Threonine Kinases (genetics), Supranuclear Palsy, Progressive (genetics), Young Adult.
- MESH :
- chemical , genetics : Protein-Serine-Threonine Kinases.
- chemical : Leucine-Rich Repeat Serine-Threonine Protein Kinase-2.
- genetics : Exons, Genetic Predisposition to Disease, Mutation, Parkinsonian Disorders, Supranuclear Palsy, Progressive.
- Adult, Aged, Aged, 80 and over, Cross-Cultural Comparison, DNA Mutational Analysis, Female, Genotype, Humans, Male, Middle Aged, Young Adult.
DOI: 10.1016/j.parkreldis.2015.07.011
PubMed: 26213354
Links to Exploration step
pubmed:26213354Le document en format XML
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<author><name sortKey="Jeon, Beom S" sort="Jeon, Beom S" uniqKey="Jeon B" first="Beom S" last="Jeon">Beom S. Jeon</name>
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<author><name sortKey="Szu Tu, Chelsea" sort="Szu Tu, Chelsea" uniqKey="Szu Tu C" first="Chelsea" last="Szu-Tu">Chelsea Szu-Tu</name>
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<author><name sortKey="Rajput, Alex" sort="Rajput, Alex" uniqKey="Rajput A" first="Alex" last="Rajput">Alex Rajput</name>
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<author><name sortKey="Rajput, Ali H" sort="Rajput, Ali H" uniqKey="Rajput A" first="Ali H" last="Rajput">Ali H. Rajput</name>
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<author><name sortKey="Mckeown, Martin" sort="Mckeown, Martin" uniqKey="Mckeown M" first="Martin" last="Mckeown">Martin Mckeown</name>
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<author><name sortKey="Jeon, Beom S" sort="Jeon, Beom S" uniqKey="Jeon B" first="Beom S" last="Jeon">Beom S. Jeon</name>
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<author><name sortKey="Aasly, Jan O" sort="Aasly, Jan O" uniqKey="Aasly J" first="Jan O" last="Aasly">Jan O. Aasly</name>
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</affiliation>
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<author><name sortKey="Bardien, Soraya" sort="Bardien, Soraya" uniqKey="Bardien S" first="Soraya" last="Bardien">Soraya Bardien</name>
<affiliation><nlm:affiliation>Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.</nlm:affiliation>
</affiliation>
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<author><name sortKey="Farrer, Matthew J" sort="Farrer, Matthew J" uniqKey="Farrer M" first="Matthew J" last="Farrer">Matthew J. Farrer</name>
<affiliation><nlm:affiliation>Djavad Mowafaghian Centre for Brain Health, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada; Pacific Parkinson's Research Centre, Department of Medicine (Neurology), University of British Columbia, Vancouver, BC, Canada.</nlm:affiliation>
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