18413475

Source:http://linkedlifedata.com/resource/pubmed/id/18413475

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0019425, umls-concept:C0019904, umls-concept:C0030705, umls-concept:C0242422, umls-concept:C0332597, umls-concept:C0497327, umls-concept:C1420276
pubmed:issue	4
pubmed:dateCreated	2008-4-16
pubmed:abstractText	Multiplication of the alpha-synuclein gene (SNCA) (OMIM 163890) has been identified as a causative mutation in hereditary Parkinson disease or dementia with Lewy bodies.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/SNCA protein, human, http://linkedlifedata.com/resource/pubmed/chemical/alpha-Synuclein
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1538-3687
pubmed:author	pubmed-author:IdezukaJiroJ, pubmed-author:IkeuchiTakeshiT, pubmed-author:IshikawaAtsushiA, pubmed-author:IwatsuboTakeshiT, pubmed-author:KakitaAkiyoshiA, pubmed-author:KanekoHiryoyukiH, pubmed-author:KasugaKensakuK, pubmed-author:NishizawaMasatoyoM, pubmed-author:OnoderaOsamuO, pubmed-author:ShigaAtsushiA, pubmed-author:TakahashiHitoshiH, pubmed-author:TanChun-FengCF, pubmed-author:WakabayashiKoichiK
pubmed:issnType	Electronic
pubmed:volume	65
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	514-9
pubmed:meshHeading	pubmed-meshheading:18413475-Age of Onset, pubmed-meshheading:18413475-Aged, pubmed-meshheading:18413475-Alleles, pubmed-meshheading:18413475-Brain, pubmed-meshheading:18413475-Cognition Disorders, pubmed-meshheading:18413475-Consanguinity, pubmed-meshheading:18413475-DNA Mutational Analysis, pubmed-meshheading:18413475-Exons, pubmed-meshheading:18413475-Female, pubmed-meshheading:18413475-Gene Dosage, pubmed-meshheading:18413475-Gene Duplication, pubmed-meshheading:18413475-Heterozygote Detection, pubmed-meshheading:18413475-Homozygote, pubmed-meshheading:18413475-Humans, pubmed-meshheading:18413475-Lewy Bodies, pubmed-meshheading:18413475-Lewy Body Disease, pubmed-meshheading:18413475-Male, pubmed-meshheading:18413475-Microsatellite Repeats, pubmed-meshheading:18413475-Middle Aged, pubmed-meshheading:18413475-Neuropsychological Tests, pubmed-meshheading:18413475-Parkinsonian Disorders, pubmed-meshheading:18413475-Phosphorylation, pubmed-meshheading:18413475-alpha-Synuclein
pubmed:year	2008
pubmed:articleTitle	Patients homozygous and heterozygous for SNCA duplication in a family with parkinsonism and dementia.
pubmed:affiliation	Department of Molecular Neuroscience, Brain Research Institute, Niigata University, 1 Asahimachi, Niigata 951-8585, Japan. ikeuchi@bri.niigata-u.ac.jp
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't