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| pubmed-article:17420318 | lifeskim:mentions | umls-concept:C1335439 | lld:lifeskim |
| pubmed-article:17420318 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:17420318 | pubmed:dateCreated | 2007-4-10 | lld:pubmed |
| pubmed-article:17420318 | pubmed:abstractText | To define the molecular basis of the autosomal dominant progressive external ophthalmoplegia and parkinsonism in a large family with a dominantly transmitted multiple mitochondrial DNA deletion disorder. | lld:pubmed |
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| pubmed-article:17420318 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:17420318 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:17420318 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17420318 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:17420318 | pubmed:issn | 0003-9942 | lld:pubmed |
| pubmed-article:17420318 | pubmed:author | pubmed-author:TaylorRobert... | lld:pubmed |
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| pubmed-article:17420318 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17420318 | pubmed:volume | 64 | lld:pubmed |
| pubmed-article:17420318 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17420318 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17420318 | pubmed:pagination | 553-7 | lld:pubmed |
| pubmed-article:17420318 | pubmed:dateRevised | 2007-8-13 | lld:pubmed |
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| pubmed-article:17420318 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17420318 | pubmed:articleTitle | Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism. | lld:pubmed |
| pubmed-article:17420318 | pubmed:affiliation | Mitochondrial Research Group, University of Newcastle upon Tyne, United Kingdom. | lld:pubmed |
| pubmed-article:17420318 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17420318 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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