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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-8-24
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pubmed:abstractText |
By using a combination of Southern blot hybridization analysis, polymerase-chain reaction amplification, and direct nucleotide sequencing, we studied deletions of mitochondrial DNA (mtDNA) in several nonfamilial patients with progressive external ophthalmoplegia and Kearns-Sayre syndrome, and in some of their direct relatives. Results suggest that the heteroplasmic mtDNA populations are already present at a very early stage of development, and that there is no direct transmission of mtDNA heteroplasmy by maternal inheritance.
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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 |
Jul
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pubmed:issn |
0364-5134
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
94-7
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:2375642-Base Sequence,
pubmed-meshheading:2375642-Blotting, Southern,
pubmed-meshheading:2375642-DNA, Mitochondrial,
pubmed-meshheading:2375642-Humans,
pubmed-meshheading:2375642-Kearns-Sayre Syndrome,
pubmed-meshheading:2375642-Molecular Sequence Data,
pubmed-meshheading:2375642-Ophthalmoplegia,
pubmed-meshheading:2375642-Polymerase Chain Reaction,
pubmed-meshheading:2375642-Tissue Distribution
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pubmed:year |
1990
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pubmed:articleTitle |
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathies.
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pubmed:affiliation |
Department of Biochemistry and Genetics, Istituto Nazionale Neurologico, Carlo Besta, Milan, Italy.
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pubmed:publicationType |
Journal Article
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