15477547

Source:http://linkedlifedata.com/resource/pubmed/id/15477547

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004134, umls-concept:C0026845, umls-concept:C0026882, umls-concept:C0524851, umls-concept:C1314939, umls-concept:C1418731
pubmed:issue	7
pubmed:dateCreated	2004-10-12
pubmed:abstractText	To identify POLG mutations in patients with sensory ataxia and CNS features.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0401060
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Directed DNA Polymerase, http://linkedlifedata.com/resource/pubmed/chemical/POLG protein, human
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	1526-632X
pubmed:author	pubmed-author:Al MemarAA, pubmed-author:De JonghePP, pubmed-author:HackmanPP, pubmed-author:KaakkolaSS, pubmed-author:KraheRR, pubmed-author:LöfgrenAA, pubmed-author:LuomaPP, pubmed-author:MartinJ JJJ, pubmed-author:RantamäkiMM, pubmed-author:SuomalainenAA, pubmed-author:UddBB, pubmed-author:Van BroeckhovenCC, pubmed-author:Van GoethemGG
pubmed:issnType	Electronic
pubmed:day	12
pubmed:volume	63
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1251-7
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:15477547-Adolescent, pubmed-meshheading:15477547-Adult, pubmed-meshheading:15477547-Aged, pubmed-meshheading:15477547-Ataxia, pubmed-meshheading:15477547-Brain, pubmed-meshheading:15477547-DNA, Mitochondrial, pubmed-meshheading:15477547-DNA-Directed DNA Polymerase, pubmed-meshheading:15477547-Female, pubmed-meshheading:15477547-Humans, pubmed-meshheading:15477547-Male, pubmed-meshheading:15477547-Middle Aged, pubmed-meshheading:15477547-Muscles, pubmed-meshheading:15477547-Mutation, pubmed-meshheading:15477547-Mutation, Missense, pubmed-meshheading:15477547-Neurodegenerative Diseases, pubmed-meshheading:15477547-Ophthalmoplegia, Chronic Progressive External, pubmed-meshheading:15477547-Pedigree, pubmed-meshheading:15477547-Point Mutation
pubmed:year	2004
pubmed:articleTitle	POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.
pubmed:affiliation	Division of Neurology and the Neuromuscular Reference Center, University Hospital, Antwerpen, Belgium. gert.vangoethem@ua.ac.be
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't