| pubmed-article:11527955 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0086418 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0035334 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0015127 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0443147 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C1314792 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C1414820 | lld:lifeskim |
| pubmed-article:11527955 | lifeskim:mentions | umls-concept:C0060081 | lld:lifeskim |
| pubmed-article:11527955 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:11527955 | pubmed:dateCreated | 2001-8-30 | lld:pubmed |
| pubmed-article:11527955 | pubmed:abstractText | To characterize the clinical features of 14 Japanese patients with autosomal dominant retinitis pigmentosa (ADRP) who were found to have a mutation in the FSCN2 gene. | lld:pubmed |
| pubmed-article:11527955 | pubmed:language | eng | lld:pubmed |
| pubmed-article:11527955 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:11527955 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:11527955 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11527955 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:11527955 | pubmed:issn | 0146-0404 | lld:pubmed |
| pubmed-article:11527955 | pubmed:author | pubmed-author:AbeTT | lld:pubmed |
| pubmed-article:11527955 | pubmed:author | pubmed-author:SatoHH | lld:pubmed |
| pubmed-article:11527955 | pubmed:author | pubmed-author:WadaYY | lld:pubmed |
| pubmed-article:11527955 | pubmed:author | pubmed-author:TamaiMM | lld:pubmed |
| pubmed-article:11527955 | pubmed:author | pubmed-author:TakeshitaTT | lld:pubmed |
| pubmed-article:11527955 | pubmed:author | pubmed-author:YanashimaKK | lld:pubmed |
| pubmed-article:11527955 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11527955 | pubmed:volume | 42 | lld:pubmed |
| pubmed-article:11527955 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11527955 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11527955 | pubmed:pagination | 2395-400 | lld:pubmed |
| pubmed-article:11527955 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:11527955 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11527955 | pubmed:articleTitle | Mutation of human retinal fascin gene (FSCN2) causes autosomal dominant retinitis pigmentosa. | lld:pubmed |
| pubmed-article:11527955 | pubmed:affiliation | Department of Ophthalmology, Tohoku University School of Medicine, Sendai, Japan. yukow@oph.med.tohoku.ac.jp | lld:pubmed |
| pubmed-article:11527955 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11527955 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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