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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2007-4-12
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pubmed:abstractText |
Mitochondrial DNA (mtDNA) mutations have been proposed as a genetic risk factor for sudden infant death syndrome (SIDS). The aim of this study was to further investigate this issue, by sequencing the mitochondrial tRNA genes with flanking regions in SIDS cases and controls.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0803-5253
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
96
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
211-4
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pubmed:meshHeading |
pubmed-meshheading:17429907-3' Flanking Region,
pubmed-meshheading:17429907-5' Flanking Region,
pubmed-meshheading:17429907-Case-Control Studies,
pubmed-meshheading:17429907-Female,
pubmed-meshheading:17429907-Genes, Mitochondrial,
pubmed-meshheading:17429907-Genetic Predisposition to Disease,
pubmed-meshheading:17429907-Humans,
pubmed-meshheading:17429907-Infant,
pubmed-meshheading:17429907-Infant, Newborn,
pubmed-meshheading:17429907-Male,
pubmed-meshheading:17429907-Mutation,
pubmed-meshheading:17429907-RNA,
pubmed-meshheading:17429907-RNA, Transfer,
pubmed-meshheading:17429907-Sudden Infant Death
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pubmed:year |
2007
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pubmed:articleTitle |
Mitochondrial tRNA genes and flanking regions in sudden infant death syndrome.
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pubmed:affiliation |
Institute of Forensic Medicine, University of Oslo, Oslo, Norway. s.h.opdal@medisin.uio.no
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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