| pubmed-article:16804265 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C1553355 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C0205101 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C0012929 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C1261322 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C0205329 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:16804265 | lifeskim:mentions | umls-concept:C0205191 | lld:lifeskim |
| pubmed-article:16804265 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:16804265 | pubmed:dateCreated | 2006-6-28 | lld:pubmed |
| pubmed-article:16804265 | pubmed:abstractText | Chronic progressive external ophthalmoplagia (CPEO) is a phenotypic mitochondrial disorder that affects external ocular and skeletal muscles and is associated with a single or multiple mitochondrial DNA (mtDNA) deletions and also nuclear gene mutations. There are also some reports about the relationship between CPEO and the nuclear Twinkle gene which encodes a kind of mitochondrial protein called Twinkle. | lld:pubmed |
| pubmed-article:16804265 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16804265 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16804265 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16804265 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16804265 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16804265 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16804265 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16804265 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16804265 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:16804265 | pubmed:issn | 0028-3886 | lld:pubmed |
| pubmed-article:16804265 | pubmed:author | pubmed-author:HoushmandMass... | lld:pubmed |
| pubmed-article:16804265 | pubmed:author | pubmed-author:PanahiM... | lld:pubmed |
| pubmed-article:16804265 | pubmed:author | pubmed-author:HosseiniB NBN | lld:pubmed |
| pubmed-article:16804265 | pubmed:author | pubmed-author:DorrajG HGH | lld:pubmed |
| pubmed-article:16804265 | pubmed:author | pubmed-author:TabassiA RAR | lld:pubmed |
| pubmed-article:16804265 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:16804265 | pubmed:volume | 54 | lld:pubmed |
| pubmed-article:16804265 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16804265 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16804265 | pubmed:pagination | 182-5 | lld:pubmed |
| pubmed-article:16804265 | pubmed:dateRevised | 2010-6-2 | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:meshHeading | pubmed-meshheading:16804265... | lld:pubmed |
| pubmed-article:16804265 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16804265 | pubmed:articleTitle | Investigation on mtDNA deletions and twinkle gene mutation (G1423C) in Iranian patients with chronic progressive external opthalmoplagia. | lld:pubmed |
| pubmed-article:16804265 | pubmed:affiliation | Department of Medical Genetics, National Institute for Genetic Engineering and Biotechnology (NIGEB), Tehran, Iran. massoudh@nrcgeb.ac.ir | lld:pubmed |
| pubmed-article:16804265 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16804265 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16804265 | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16804265 | lld:pubmed |
