| pubmed-article:11074292 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11074292 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
| pubmed-article:11074292 | lifeskim:mentions | umls-concept:C0728826 | lld:lifeskim |
| pubmed-article:11074292 | lifeskim:mentions | umls-concept:C0036576 | lld:lifeskim |
| pubmed-article:11074292 | lifeskim:mentions | umls-concept:C0439605 | lld:lifeskim |
| pubmed-article:11074292 | pubmed:issue | 11 | lld:pubmed |
| pubmed-article:11074292 | pubmed:dateCreated | 2000-12-4 | lld:pubmed |
| pubmed-article:11074292 | 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. | lld:pubmed |
| pubmed-article:11074292 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11074292 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11074292 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:11074292 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11074292 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11074292 | pubmed:month | Nov | lld:pubmed |
| pubmed-article:11074292 | pubmed:issn | 0168-9525 | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:WhiteS LSL | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:HowellNN | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:TurnbullD MDM | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:LightowlersR... | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:ThorburnD RDR | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:ChinneryP FPF | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:DahlH MHM | lld:pubmed |
| pubmed-article:11074292 | pubmed:author | pubmed-author:SamuelsD CDC | lld:pubmed |
| pubmed-article:11074292 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11074292 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:11074292 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11074292 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11074292 | pubmed:pagination | 500-5 | lld:pubmed |
| pubmed-article:11074292 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:11074292 | pubmed:meshHeading | pubmed-meshheading:11074292... | lld:pubmed |
| pubmed-article:11074292 | pubmed:year | 2000 | lld:pubmed |
| pubmed-article:11074292 | pubmed:articleTitle | The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both? | lld:pubmed |
| pubmed-article:11074292 | pubmed:affiliation | Department of Neurology, The Medical School, NE2 4HH., Newcastle upon Tyne, UK. | lld:pubmed |
| pubmed-article:11074292 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11074292 | pubmed:publicationType | Research Support, U.S. Gov't, Non-P.H.S. | lld:pubmed |
| pubmed-article:11074292 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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