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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
1999-3-18
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pubmed:abstractText |
To develop a protocol capable of identifying deletions in mitochondrial DNA and use it to identify the breakpoints of a mtDNA deletion in a patient with chronic progressive external ophthalmoplegia (CPEO).
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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 |
Nov
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pubmed:issn |
0009-9120
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
627-32
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:9876894-Adolescent,
pubmed-meshheading:9876894-Blepharoptosis,
pubmed-meshheading:9876894-Blotting, Southern,
pubmed-meshheading:9876894-DNA, Mitochondrial,
pubmed-meshheading:9876894-Humans,
pubmed-meshheading:9876894-Kearns-Sayre Syndrome,
pubmed-meshheading:9876894-Male,
pubmed-meshheading:9876894-Mitochondrial Encephalomyopathies,
pubmed-meshheading:9876894-Ophthalmoplegia,
pubmed-meshheading:9876894-Ophthalmoplegia, Chronic Progressive External,
pubmed-meshheading:9876894-Polymerase Chain Reaction,
pubmed-meshheading:9876894-Sensitivity and Specificity,
pubmed-meshheading:9876894-Sequence Deletion
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pubmed:year |
1998
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pubmed:articleTitle |
A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletion.
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pubmed:affiliation |
Department of Pediatrics, University of British Columbia, Vancouver, Canada. marioncm@interchange.ubc.ca
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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