Source:http://linkedlifedata.com/resource/pubmed/id/11074292
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
11
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pubmed:dateCreated |
2000-12-4
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pubmed:abstractText |
The mammalian mitochondrial genome (mtDNA) is a small double-stranded DNA molecule that is exclusively transmitted down the maternal line. Pathogenic mtDNA mutations are usually heteroplasmic, with a mixture of mutant and wild-type mtDNA within the same organism. A woman harbouring one of these mutations transmits a variable amount of mutant mtDNA to each offspring. This can result in a healthy child or an infant with a devastating and fatal neurological disorder. Understanding the biological basis of this uncertainty is one of the principal challenges facing scientists and clinicians in the field of mitochondrial genetics.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
0168-9525
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
500-5
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:11074292-Animals,
pubmed-meshheading:11074292-DNA, Mitochondrial,
pubmed-meshheading:11074292-Female,
pubmed-meshheading:11074292-Gene Frequency,
pubmed-meshheading:11074292-Humans,
pubmed-meshheading:11074292-Mice,
pubmed-meshheading:11074292-Mutation,
pubmed-meshheading:11074292-Polymorphism, Genetic,
pubmed-meshheading:11074292-Selection, Genetic,
pubmed-meshheading:11074292-Species Specificity
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pubmed:year |
2000
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pubmed:articleTitle |
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?
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pubmed:affiliation |
Department of Neurology, The Medical School, NE2 4HH., Newcastle upon Tyne, UK.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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