| pubmed-article:21203403 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21203403 | lifeskim:mentions | umls-concept:C0917796 | lld:lifeskim |
| pubmed-article:21203403 | lifeskim:mentions | umls-concept:C0205419 | lld:lifeskim |
| pubmed-article:21203403 | lifeskim:mentions | umls-concept:C1417953 | lld:lifeskim |
| pubmed-article:21203403 | lifeskim:mentions | umls-concept:C1836598 | lld:lifeskim |
| pubmed-article:21203403 | pubmed:dateCreated | 2011-1-4 | lld:pubmed |
| pubmed-article:21203403 | pubmed:abstractText | Leber hereditary optic neuropathy (LHON) is a common cause of inherited blindness, primarily due to one of three mitochondrial DNA (mtDNA) mutations. These mtDNA pathogenic mutations have variable clinical penetrance. Recent linkage evidence raised the possibility that the nuclear gene optic atrophy 1 (OPA1) determines whether mtDNA mutation carriers develop blindness. To validate these findings we studied OPA1 in three independent LHON cohorts: sequencing the gene in discordant male sib pairs, carrying out a family-based association study of common functional genetic variants, and carrying out a population-based association study of the same genetic variants. | lld:pubmed |
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| pubmed-article:21203403 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21203403 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21203403 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21203403 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21203403 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21203403 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21203403 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21203403 | pubmed:issn | 1090-0535 | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:ZevianiMassim... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:CarelliValeri... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:ChinneryPatri... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:BerezovskyAdr... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:HudsonGavinG | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:Yu-Wai-ManPat... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:CaporaliLeona... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:GriffithsPhil... | lld:pubmed |
| pubmed-article:21203403 | pubmed:author | pubmed-author:SalomaoSolang... | lld:pubmed |
| pubmed-article:21203403 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21203403 | pubmed:volume | 16 | lld:pubmed |
| pubmed-article:21203403 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21203403 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21203403 | pubmed:pagination | 2760-4 | lld:pubmed |
| pubmed-article:21203403 | pubmed:dateRevised | 2011-7-20 | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:meshHeading | pubmed-meshheading:21203403... | lld:pubmed |
| pubmed-article:21203403 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:21203403 | pubmed:articleTitle | Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy. | lld:pubmed |
| pubmed-article:21203403 | pubmed:affiliation | Institute for Human Genetics, Newcastle University, Newcastle upon Tyne, UK. | lld:pubmed |
| pubmed-article:21203403 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21203403 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:4976 | entrezgene:pubmed | pubmed-article:21203403 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21203403 | lld:entrezgene |
