|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0012929,
umls-concept:C0017337,
umls-concept:C0030013,
umls-concept:C0030705,
umls-concept:C0035711,
umls-concept:C0242692,
umls-concept:C0243067,
umls-concept:C0936012,
umls-concept:C1441616,
umls-concept:C1537998,
umls-concept:C1704241,
umls-concept:C2700640
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|
pubmed:issue |
2
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|
pubmed:dateCreated |
2009-2-2
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|
pubmed:abstractText |
Mitochondrial diseases display a heterogeneous spectrum of clinical phenotypes and therefore the identification of the underlying gene defect is often a difficult task.
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pubmed:language |
eng
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pubmed:journal |
|
|
pubmed:citationSubset |
AIM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
|
|
pubmed:issn |
1472-4146
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pubmed:author |
|
|
pubmed:issnType |
Electronic
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pubmed:volume |
62
|
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pubmed:owner |
NLM
|
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pubmed:authorsComplete |
Y
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pubmed:pagination |
172-6
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pubmed:meshHeading |
pubmed-meshheading:19181635-Adult,
pubmed-meshheading:19181635-Biological Markers,
pubmed-meshheading:19181635-DNA, Mitochondrial,
pubmed-meshheading:19181635-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:19181635-Female,
pubmed-meshheading:19181635-Humans,
pubmed-meshheading:19181635-Immunoenzyme Techniques,
pubmed-meshheading:19181635-Infant,
pubmed-meshheading:19181635-Male,
pubmed-meshheading:19181635-Middle Aged,
pubmed-meshheading:19181635-Mitochondrial Myopathies,
pubmed-meshheading:19181635-Multienzyme Complexes,
pubmed-meshheading:19181635-Muscle, Skeletal,
pubmed-meshheading:19181635-Mutation,
pubmed-meshheading:19181635-Oxidative Phosphorylation,
pubmed-meshheading:19181635-RNA, Transfer
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|
pubmed:year |
2009
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|
pubmed:articleTitle |
Immunohistochemical analysis of the oxidative phosphorylation complexes in skeletal muscle from patients with mitochondrial DNA encoded tRNA gene defects.
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pubmed:affiliation |
Department of Pediatric Neurology & Metabolism, University Hospital, Ghent, Belgium. boel.depaepe@ugent.be
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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