| Home > Publications Database > No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease. > print |
| 001 | 141166 | ||
| 005 | 20240321220930.0 | ||
| 024 | 7 | _ | |a 10.1002/mds.25330 |2 doi |
| 024 | 7 | _ | |a pmid:23390085 |2 pmid |
| 024 | 7 | _ | |a pmc:PMC3766482 |2 pmc |
| 024 | 7 | _ | |a 0885-3185 |2 ISSN |
| 024 | 7 | _ | |a 1531-8257 |2 ISSN |
| 037 | _ | _ | |a DZNE-2020-07488 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 610 |
| 100 | 1 | _ | |a Appenzeller, Silke |0 P:(DE-HGF)0 |b 0 |
| 245 | _ | _ | |a No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's disease. |
| 260 | _ | _ | |a New York, NY |c 2013 |b Wiley |
| 264 | _ | 1 | |3 online |2 Crossref |b Wiley |c 2013-02-06 |
| 264 | _ | 1 | |3 print |2 Crossref |b Wiley |c 2013-08-01 |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1591090446_4413 |2 PUB:(DE-HGF) |x Letter |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 536 | _ | _ | |a 345 - Population Studies and Genetics (POF3-345) |0 G:(DE-HGF)POF3-345 |c POF3-345 |f POF III |x 0 |
| 542 | _ | _ | |i 2015-09-01 |2 Crossref |u http://doi.wiley.com/10.1002/tdm_license_1.1 |
| 588 | _ | _ | |a Dataset connected to CrossRef, PubMed, |
| 650 | _ | 7 | |a Glutamate Plasma Membrane Transport Proteins |2 NLM Chemicals |
| 650 | _ | 7 | |a SLC1A2 protein, human |2 NLM Chemicals |
| 650 | _ | 2 | |a Essential Tremor: genetics |2 MeSH |
| 650 | _ | 2 | |a Female |2 MeSH |
| 650 | _ | 2 | |a Genetic Association Studies |2 MeSH |
| 650 | _ | 2 | |a Germany |2 MeSH |
| 650 | _ | 2 | |a Glutamate Plasma Membrane Transport Proteins: genetics |2 MeSH |
| 650 | _ | 2 | |a Humans |2 MeSH |
| 650 | _ | 2 | |a Male |2 MeSH |
| 650 | _ | 2 | |a Parkinson Disease: genetics |2 MeSH |
| 650 | _ | 2 | |a Polymorphism, Single Nucleotide: genetics |2 MeSH |
| 650 | _ | 2 | |a United States |2 MeSH |
| 700 | 1 | _ | |a Schulte, Claudia |0 P:(DE-HGF)0 |b 1 |
| 700 | 1 | _ | |a Thier, Sandra |0 P:(DE-HGF)0 |b 2 |
| 700 | 1 | _ | |a Hopfner, Franziska |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Pendziwiat, Manuela |0 P:(DE-HGF)0 |b 4 |
| 700 | 1 | _ | |a Papengut, Frank |0 P:(DE-HGF)0 |b 5 |
| 700 | 1 | _ | |a Klein, Christine |0 P:(DE-HGF)0 |b 6 |
| 700 | 1 | _ | |a Hagenah, Johann |0 P:(DE-HGF)0 |b 7 |
| 700 | 1 | _ | |a Kasten, Meike |0 P:(DE-HGF)0 |b 8 |
| 700 | 1 | _ | |a Srulijes, Karin |0 P:(DE-2719)9000298 |b 9 |u dzne |
| 700 | 1 | _ | |a Berg, Daniela |0 P:(DE-2719)2000059 |b 10 |u dzne |
| 700 | 1 | _ | |a Gasser, Thomas |0 P:(DE-2719)2320009 |b 11 |u dzne |
| 700 | 1 | _ | |a Singleton, Andrew |0 P:(DE-HGF)0 |b 12 |
| 700 | 1 | _ | |a Deuschl, Günther |0 P:(DE-HGF)0 |b 13 |
| 700 | 1 | _ | |a Kuhlenbäumer, Gregor |0 P:(DE-HGF)0 |b 14 |e Corresponding author |
| 773 | 1 | 8 | |a 10.1002/mds.25330 |b : Wiley, 2013-02-06 |n 9 |p 1305-1306 |3 journal-article |2 Crossref |t Movement Disorders |v 28 |y 2013 |x 0885-3185 |
| 773 | _ | _ | |a 10.1002/mds.25330 |g Vol. 28, no. 9, p. 1305 - 1306 |0 PERI:(DE-600)2041249-6 |n 9 |q 28:9<1305 - 1306 |p 1305-1306 |t Movement disorders |v 28 |y 2013 |x 0885-3185 |
| 856 | 7 | _ | |2 Pubmed Central |u http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766482 |
| 909 | C | O | |o oai:pub.dzne.de:141166 |p VDB |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 9 |6 P:(DE-2719)9000298 |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 10 |6 P:(DE-2719)2000059 |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 11 |6 P:(DE-2719)2320009 |
| 913 | 1 | _ | |a DE-HGF |b Forschungsbereich Gesundheit |l Erkrankungen des Nervensystems |1 G:(DE-HGF)POF3-340 |0 G:(DE-HGF)POF3-345 |2 G:(DE-HGF)POF3-300 |v Population Studies and Genetics |x 0 |
| 914 | 1 | _ | |y 2013 |
| 915 | _ | _ | |a Nationallizenz |0 StatID:(DE-HGF)0420 |2 StatID |
| 915 | _ | _ | |a JCR |0 StatID:(DE-HGF)0100 |2 StatID |b MOVEMENT DISORD : 2017 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0300 |2 StatID |b Medline |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0310 |2 StatID |b NCBI Molecular Biology Database |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0199 |2 StatID |b Clarivate Analytics Master Journal List |
| 915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0110 |2 StatID |b Science Citation Index |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0150 |2 StatID |b Web of Science Core Collection |
| 915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0111 |2 StatID |b Science Citation Index Expanded |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1110 |2 StatID |b Current Contents - Clinical Medicine |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1030 |2 StatID |b Current Contents - Life Sciences |
| 915 | _ | _ | |a IF >= 5 |0 StatID:(DE-HGF)9905 |2 StatID |b MOVEMENT DISORD : 2017 |
| 920 | 1 | _ | |0 I:(DE-2719)5000055 |k AG Berg |l Parkinson's Disease Genetics AG Berg |x 0 |
| 920 | 1 | _ | |0 I:(DE-2719)1210000 |k AG Gasser 1 |l Parkinson Genetics |x 1 |
| 980 | _ | _ | |a journal |
| 980 | _ | _ | |a VDB |
| 980 | _ | _ | |a I:(DE-2719)5000055 |
| 980 | _ | _ | |a I:(DE-2719)1210000 |
| 980 | _ | _ | |a UNRESTRICTED |
| 999 | C | 5 | |a 10.1016/j.parkreldis.2006.05.033 |9 -- missing cx lookup -- |2 Crossref |o 10.1016/j.parkreldis.2006.05.033 |
| 999 | C | 5 | |a 10.1038/ng.299 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/ng.299 |
| 999 | C | 5 | |a 10.1212/WNL.0b013e31825fdeed |9 -- missing cx lookup -- |2 Crossref |o 10.1212/WNL.0b013e31825fdeed |
| 999 | C | 5 | |y 2010 |2 Crossref |o Klebe 2010 |
| 999 | C | 5 | |a 10.1086/519795 |9 -- missing cx lookup -- |2 Crossref |o 10.1086/519795 |
| 999 | C | 5 | |a 10.1038/ng.487 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/ng.487 |
| 999 | C | 5 | |a 10.1111/j.1600-0404.2011.01516.x |9 -- missing cx lookup -- |2 Crossref |o 10.1111/j.1600-0404.2011.01516.x |
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