19001169

Source:http://linkedlifedata.com/resource/pubmed/id/19001169

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:C0023520, umls-concept:C0205314, umls-concept:C0332597, umls-concept:C0443147, umls-concept:C0679622, umls-concept:C1314939, umls-concept:C1456348, umls-concept:C1521484
pubmed:issue	11
pubmed:dateCreated	2008-11-12
pubmed:abstractText	To identify the underlying locus and disease-causing mutation for adult-onset autosomal dominant leukodystrophy (ADLD).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372436
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Lamin Type B, http://linkedlifedata.com/resource/pubmed/chemical/lamin B1
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1538-3687
pubmed:author	pubmed-author:BouchardJean-PierreJP, pubmed-author:DupréNicolasN, pubmed-author:KatzTanyaT, pubmed-author:LaurentSandraS, pubmed-author:MathurinJohanneJ, pubmed-author:MeijerInge AIA, pubmed-author:RouleauGuy AGA, pubmed-author:Simoes-LopesAna AAA, pubmed-author:St-OngeJudithJ, pubmed-author:ThibaultManonM, pubmed-author:VerlaanDominique JDJ
pubmed:issnType	Electronic
pubmed:volume	65
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1496-501
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:19001169-Aged, pubmed-meshheading:19001169-Brain, pubmed-meshheading:19001169-Canada, pubmed-meshheading:19001169-Chromosome Mapping, pubmed-meshheading:19001169-Chromosomes, Human, Pair 5, pubmed-meshheading:19001169-Comparative Genomic Hybridization, pubmed-meshheading:19001169-Female, pubmed-meshheading:19001169-Genes, Dominant, pubmed-meshheading:19001169-Genes, Duplicate, pubmed-meshheading:19001169-Genetic Linkage, pubmed-meshheading:19001169-Genotype, pubmed-meshheading:19001169-Haplotypes, pubmed-meshheading:19001169-Hereditary Central Nervous System Demyelinating Diseases, pubmed-meshheading:19001169-Humans, pubmed-meshheading:19001169-Lamin Type B, pubmed-meshheading:19001169-Magnetic Resonance Imaging, pubmed-meshheading:19001169-Male, pubmed-meshheading:19001169-Middle Aged, pubmed-meshheading:19001169-Neurodegenerative Diseases, pubmed-meshheading:19001169-Pedigree
pubmed:year	2008
pubmed:articleTitle	A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.
pubmed:affiliation	Centre of Excellence in Neuromics, Centre Hospitalier de l'Université de Montreal and Ste-Justine Hospital, Montreal, Canada.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't