|
rdf:type |
|
|
lifeskim:mentions |
|
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pubmed:issue |
5
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|
pubmed:dateCreated |
2007-4-24
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pubmed:abstractText |
To determine the actual incidence of mitochondrial DNA (mtDNA) depletion syndrome in multiple respiratory chain deficiency.
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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 |
May
|
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pubmed:issn |
1097-6833
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:volume |
150
|
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pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
531-4, 534.e1-6
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pubmed:meshHeading |
pubmed-meshheading:17452231-Child, Preschool,
pubmed-meshheading:17452231-DNA, Mitochondrial,
pubmed-meshheading:17452231-Female,
pubmed-meshheading:17452231-Humans,
pubmed-meshheading:17452231-Infant,
pubmed-meshheading:17452231-Infant, Newborn,
pubmed-meshheading:17452231-Liver,
pubmed-meshheading:17452231-Male,
pubmed-meshheading:17452231-Mitochondrial Diseases,
pubmed-meshheading:17452231-Muscle, Skeletal
|
|
pubmed:year |
2007
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|
pubmed:articleTitle |
Mitochondrial DNA depletion is a prevalent cause of multiple respiratory chain deficiency in childhood.
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|
pubmed:affiliation |
INSERM U781, Hôpital Necker-Enfants Malades, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
