141166 20240321220930.0 10.1002/mds.25330 doi pmid:23390085 pmid pmc:PMC3766482 pmc 0885-3185 ISSN 1531-8257 ISSN DZNE-2020-07488 English 610 Appenzeller, Silke P:(DE-HGF)0 0 No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease. New York, NY 2013 Wiley online Crossref Wiley 2013-02-06 print Crossref Wiley 2013-08-01 article DRIVER Output Types/Journal article DataCite Journal Article journal journal PUB:(DE-HGF)16 1591090446_4413 PUB:(DE-HGF) Letter ARTICLE BibTeX JOURNAL_ARTICLE ORCID Journal Article 0 EndNote 345 - Population Studies and Genetics (POF3-345) G:(DE-HGF)POF3-345 POF3-345 POF III 0 2015-09-01 Crossref http://doi.wiley.com/10.1002/tdm_license_1.1 Dataset connected to CrossRef, PubMed, Glutamate Plasma Membrane Transport Proteins NLM Chemicals SLC1A2 protein, human NLM Chemicals Essential Tremor: genetics MeSH Female MeSH Genetic Association Studies MeSH Germany MeSH Glutamate Plasma Membrane Transport Proteins: genetics MeSH Humans MeSH Male MeSH Parkinson Disease: genetics MeSH Polymorphism, Single Nucleotide: genetics MeSH United States MeSH Schulte, Claudia P:(DE-HGF)0 1 Thier, Sandra P:(DE-HGF)0 2 Hopfner, Franziska P:(DE-HGF)0 3 Pendziwiat, Manuela P:(DE-HGF)0 4 Papengut, Frank P:(DE-HGF)0 5 Klein, Christine P:(DE-HGF)0 6 Hagenah, Johann P:(DE-HGF)0 7 Kasten, Meike P:(DE-HGF)0 8 Srulijes, Karin P:(DE-2719)9000298 9 dzne Berg, Daniela P:(DE-2719)2000059 10 dzne Gasser, Thomas P:(DE-2719)2320009 11 dzne Singleton, Andrew P:(DE-HGF)0 12 Deuschl, Günther P:(DE-HGF)0 13 Kuhlenbäumer, Gregor P:(DE-HGF)0 14 Corresponding author 10.1002/mds.25330 : Wiley, 2013-02-06 9 1305-1306 journal-article Crossref Movement Disorders 28 2013 0885-3185 10.1002/mds.25330 Vol. 28, no. 9, p. 1305 - 1306 PERI:(DE-600)2041249-6 9 28:9<1305 - 1306 1305-1306 Movement disorders 28 2013 0885-3185 Pubmed Central http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766482 oai:pub.dzne.de:141166 VDB Deutsches Zentrum für Neurodegenerative Erkrankungen I:(DE-588)1065079516 DZNE 9 P:(DE-2719)9000298 Deutsches Zentrum für Neurodegenerative Erkrankungen I:(DE-588)1065079516 DZNE 10 P:(DE-2719)2000059 Deutsches Zentrum für Neurodegenerative Erkrankungen I:(DE-588)1065079516 DZNE 11 P:(DE-2719)2320009 DE-HGF Forschungsbereich Gesundheit Erkrankungen des Nervensystems G:(DE-HGF)POF3-340 G:(DE-HGF)POF3-345 G:(DE-HGF)POF3-300 Population Studies and Genetics 0 2013 Nationallizenz StatID:(DE-HGF)0420 StatID JCR StatID:(DE-HGF)0100 StatID MOVEMENT DISORD : 2017 DBCoverage StatID:(DE-HGF)0200 StatID SCOPUS DBCoverage StatID:(DE-HGF)0300 StatID Medline DBCoverage StatID:(DE-HGF)0310 StatID NCBI Molecular Biology Database DBCoverage StatID:(DE-HGF)0199 StatID Clarivate Analytics Master Journal List WoS StatID:(DE-HGF)0110 StatID Science Citation Index DBCoverage StatID:(DE-HGF)0150 StatID Web of Science Core Collection WoS StatID:(DE-HGF)0111 StatID Science Citation Index Expanded DBCoverage StatID:(DE-HGF)1110 StatID Current Contents - Clinical Medicine DBCoverage StatID:(DE-HGF)1030 StatID Current Contents - Life Sciences IF >= 5 StatID:(DE-HGF)9905 StatID MOVEMENT DISORD : 2017 I:(DE-2719)5000055 AG Berg Parkinson's Disease Genetics AG Berg 0 I:(DE-2719)1210000 AG Gasser 1 Parkinson Genetics 1 journal VDB I:(DE-2719)5000055 I:(DE-2719)1210000 UNRESTRICTED 10.1016/j.parkreldis.2006.05.033 -- missing cx lookup -- Crossref 10.1016/j.parkreldis.2006.05.033 10.1038/ng.299 -- missing cx lookup -- Crossref 10.1038/ng.299 10.1212/WNL.0b013e31825fdeed -- missing cx lookup -- Crossref 10.1212/WNL.0b013e31825fdeed 2010 Crossref Klebe 2010 10.1086/519795 -- missing cx lookup -- Crossref 10.1086/519795 10.1038/ng.487 -- missing cx lookup -- Crossref 10.1038/ng.487 10.1111/j.1600-0404.2011.01516.x -- missing cx lookup -- Crossref 10.1111/j.1600-0404.2011.01516.x