No association between NOD2 variants and Parkinson's disease.
Identifieur interne : 000C89 ( Main/Exploration ); précédent : 000C88; suivant : 000C90No association between NOD2 variants and Parkinson's disease.
Auteurs : Silke Appenzeller [Allemagne] ; Sandra Thier ; Frank Papengut ; Christine Klein ; Johann Hagenah ; Meike Kasten ; Daniela Berg ; Karin Srulijes ; Thomas Gasser ; Stefan Schreiber ; Günther Deuschl ; Gregor Kuhlenb UmerSource :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2012.
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Nod2 Signaling Adaptor Protein.
- genetics : Parkinson Disease.
- Aged, Genetic Variation, Genotype, Humans, Polymerase Chain Reaction, Polymorphism, Single Nucleotide.
DOI: 10.1002/mds.25059
PubMed: 22807259
Affiliations:
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Le document en format XML
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sort="Thier, Sandra" uniqKey="Thier S" first="Sandra" last="Thier">Sandra Thier</name></noCountry><country name="Allemagne"><region name="Schleswig-Holstein"><name sortKey="Appenzeller, Silke" sort="Appenzeller, Silke" uniqKey="Appenzeller S" first="Silke" last="Appenzeller">Silke Appenzeller</name></region></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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