10080174

Source:http://linkedlifedata.com/resource/pubmed/id/10080174

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0014550, umls-concept:C0015127, umls-concept:C0023520, umls-concept:C0521451, umls-concept:C0596988, umls-concept:C1314792, umls-concept:C1417652, umls-concept:C1711351, umls-concept:C2245017
pubmed:issue	3
pubmed:dateCreated	1999-3-31
pubmed:databankReference	http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AE000317, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF053070, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M58607, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X64402, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/X83999, http://linkedlifedata.com/resource/pubmed/xref/GENBANK/Z50109
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9216904
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/NAD(P)H Dehydrogenase (Quinone), http://linkedlifedata.com/resource/pubmed/chemical/NADH Dehydrogenase, http://linkedlifedata.com/resource/pubmed/chemical/NDUFV1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Proteins
pubmed:status	MEDLINE
pubmed:month	Mar
pubmed:issn	1061-4036
pubmed:author	pubmed-author:LoeffenJJ, pubmed-author:MarimanEE, pubmed-author:PleckoBB, pubmed-author:SchuelkeMM, pubmed-author:SmeitinkJJ, pubmed-author:Stöckler-IpsirogluSS, pubmed-author:TrijbelsFF, pubmed-author:van den HeuvelLL
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	260-1
pubmed:dateRevised	2007-11-15
pubmed:meshHeading	pubmed-meshheading:10080174-Amino Acid Sequence, pubmed-meshheading:10080174-Brain, pubmed-meshheading:10080174-Brain Diseases, pubmed-meshheading:10080174-Canavan Disease, pubmed-meshheading:10080174-Child, Preschool, pubmed-meshheading:10080174-Epilepsies, Myoclonic, pubmed-meshheading:10080174-Female, pubmed-meshheading:10080174-Homozygote, pubmed-meshheading:10080174-Humans, pubmed-meshheading:10080174-Infant, pubmed-meshheading:10080174-Male, pubmed-meshheading:10080174-Mitochondria, pubmed-meshheading:10080174-Molecular Sequence Data, pubmed-meshheading:10080174-Mutation, Missense, pubmed-meshheading:10080174-NAD(P)H Dehydrogenase (Quinone), pubmed-meshheading:10080174-NADH Dehydrogenase, pubmed-meshheading:10080174-Pedigree, pubmed-meshheading:10080174-Pregnancy, pubmed-meshheading:10080174-Proteins, pubmed-meshheading:10080174-Sequence Homology, Amino Acid
pubmed:year	1999
pubmed:articleTitle	Mutant NDUFV1 subunit of mitochondrial complex I causes leukodystrophy and myoclonic epilepsy.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't