9771247

Source:http://linkedlifedata.com/resource/pubmed/id/9771247

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012929, umls-concept:C0034927, umls-concept:C0200898, umls-concept:C0205210, umls-concept:C0587081
pubmed:issue	1
pubmed:dateCreated	1998-10-21
pubmed:abstractText	Increasingly, mutations of mitochondrial DNA (mtDNA) are being considered when investigating the aetiology of neurological diseases in childhood. However, they are often difficult to predict clinically.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/
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pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0372434
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, Mitochondrial
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1468-2044
pubmed:author	pubmed-author:HardingA EAE, pubmed-author:LamontP JPJ, pubmed-author:LeonardJ VJV, pubmed-author:SurteesRR, pubmed-author:WinnR HRH, pubmed-author:WoodwardC ECE
pubmed:issnType	Electronic
pubmed:volume	79
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	22-7
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:9771247-Acidosis, Lactic, pubmed-meshheading:9771247-Adolescent, pubmed-meshheading:9771247-Age of Onset, pubmed-meshheading:9771247-Cerebrovascular Disorders, pubmed-meshheading:9771247-Child, pubmed-meshheading:9771247-Child, Preschool, pubmed-meshheading:9771247-DNA, Mitochondrial, pubmed-meshheading:9771247-DNA Mutational Analysis, pubmed-meshheading:9771247-Female, pubmed-meshheading:9771247-Gene Rearrangement, pubmed-meshheading:9771247-Genotype, pubmed-meshheading:9771247-Humans, pubmed-meshheading:9771247-Infant, pubmed-meshheading:9771247-Kearns-Sayre Syndrome, pubmed-meshheading:9771247-Leigh Disease, pubmed-meshheading:9771247-Leukocytes, pubmed-meshheading:9771247-Male, pubmed-meshheading:9771247-Mitochondria, Muscle, pubmed-meshheading:9771247-Nervous System Diseases, pubmed-meshheading:9771247-Phenotype, pubmed-meshheading:9771247-Point Mutation, pubmed-meshheading:9771247-Retrospective Studies
pubmed:year	1998
pubmed:articleTitle	Clinical and laboratory findings in referrals for mitochondrial DNA analysis.
pubmed:affiliation	Neurogenetics Section, Institute of Neurology, London, UK.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't