| pubmed-article:16280978 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0086409 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0032659 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0024437 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0042333 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C1414820 | lld:lifeskim |
| pubmed-article:16280978 | lifeskim:mentions | umls-concept:C0060081 | lld:lifeskim |
| pubmed-article:16280978 | pubmed:dateCreated | 2005-11-10 | lld:pubmed |
| pubmed-article:16280978 | pubmed:abstractText | Only one mutation in the retinal fascin gene (FSCN2) has so far been associated with autosomal dominant retinitis pigmentosa (adRP) and macular dystrophy (adMD), in a Japanese population. Our study was designed to identify mutations in the FSCN2 gene among Spanish persons with adRP or adMD. | lld:pubmed |
| pubmed-article:16280978 | pubmed:language | eng | lld:pubmed |
| pubmed-article:16280978 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16280978 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:16280978 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16280978 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16280978 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16280978 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16280978 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:16280978 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16280978 | pubmed:issn | 1090-0535 | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:BaigetMontser... | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:AyusoCarmenC | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:MillánJosé... | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:AntiñoloGuill... | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:BorregoSaludS | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:GamundiMaría... | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:HernanImmaI | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:MaserasMiquel... | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:CarballoMigue... | lld:pubmed |
| pubmed-article:16280978 | pubmed:author | pubmed-author:ValverdeDiana... | lld:pubmed |
| pubmed-article:16280978 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:16280978 | pubmed:volume | 11 | lld:pubmed |
| pubmed-article:16280978 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16280978 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16280978 | pubmed:pagination | 922-8 | lld:pubmed |
| pubmed-article:16280978 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:meshHeading | pubmed-meshheading:16280978... | lld:pubmed |
| pubmed-article:16280978 | pubmed:year | 2005 | lld:pubmed |
| pubmed-article:16280978 | pubmed:articleTitle | Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration. | lld:pubmed |
| pubmed-article:16280978 | pubmed:affiliation | Laboratori de Biologia i Genetica Molecular, Hospital de Terrassa, Ctra. Torrebonica, Terrassa, Spain. | lld:pubmed |
| pubmed-article:16280978 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16280978 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:25794 | entrezgene:pubmed | pubmed-article:16280978 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:16280978 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:16280978 | lld:entrezgene |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:16280978 | lld:pubmed |
