Source:http://linkedlifedata.com/resource/pubmed/id/12013987
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
2002-5-16
|
pubmed:language |
jpn
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
0047-1852
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
60 Suppl 4
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
738-42
|
pubmed:dateRevised |
2011-7-27
|
pubmed:meshHeading |
pubmed-meshheading:12013987-Acetyl-CoA C-Acyltransferase,
pubmed-meshheading:12013987-Diagnosis, Differential,
pubmed-meshheading:12013987-Humans,
pubmed-meshheading:12013987-Mitochondria,
pubmed-meshheading:12013987-Mitochondrial Diseases,
pubmed-meshheading:12013987-Mutation,
pubmed-meshheading:12013987-Prognosis
|
pubmed:year |
2002
|
pubmed:articleTitle |
[3-ketoacyl-CoA thiolase deficiency].
|
pubmed:affiliation |
Department of Pediatrics, Gifu University School of Medicine.
|
pubmed:publicationType |
Journal Article,
Review
|