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Article: G209A mutation in the α-synuclein gene is rare and not associated with sporadic Parkinson's disease

TitleG209A mutation in the α-synuclein gene is rare and not associated with sporadic Parkinson's disease
Authors
Issue Date1998
PublisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/76507419
Citation
Movement Disorders, 1998, v. 13 n. 6, p. 970-971 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/162230
ISSN
2015 Impact Factor: 6.01
2015 SCImago Journal Rankings: 2.733
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHo, SLen_US
dc.contributor.authorKung, MHWen_US
dc.date.accessioned2012-09-05T05:18:16Z-
dc.date.available2012-09-05T05:18:16Z-
dc.date.issued1998en_US
dc.identifier.citationMovement Disorders, 1998, v. 13 n. 6, p. 970-971en_US
dc.identifier.issn0885-3185en_US
dc.identifier.urihttp://hdl.handle.net/10722/162230-
dc.languageengen_US
dc.publisherJohn Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/76507419en_US
dc.relation.ispartofMovement Disordersen_US
dc.subject.meshAge Of Onseten_US
dc.subject.meshChromosome Mappingen_US
dc.subject.meshChromosomes, Human, Pair 4en_US
dc.subject.meshDna Mutational Analysisen_US
dc.subject.meshEnglanden_US
dc.subject.meshFemaleen_US
dc.subject.meshHong Kongen_US
dc.subject.meshHumansen_US
dc.subject.meshMaleen_US
dc.subject.meshParkinson Disease - Geneticsen_US
dc.subject.meshPoint Mutationen_US
dc.subject.meshPolymerase Chain Reactionen_US
dc.titleG209A mutation in the α-synuclein gene is rare and not associated with sporadic Parkinson's diseaseen_US
dc.typeArticleen_US
dc.identifier.emailHo, SL:slho@hku.hken_US
dc.identifier.authorityHo, SL=rp00240en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1002/mds.870130619-
dc.identifier.pmid9827625en_US
dc.identifier.scopuseid_2-s2.0-0031795314en_US
dc.identifier.volume13en_US
dc.identifier.issue6en_US
dc.identifier.spage970en_US
dc.identifier.epage971en_US
dc.identifier.isiWOS:000076764700018-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridHo, SL=25959633500en_US
dc.identifier.scopusauthoridKung, MHW=36336960300en_US

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