| pubmed-article:17724221 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0012634 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0019904 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0035687 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0205082 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C1412063 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0205329 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:17724221 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:17724221 | pubmed:issue | 9 | lld:pubmed |
| pubmed-article:17724221 | pubmed:dateCreated | 2007-8-28 | lld:pubmed |
| pubmed-article:17724221 | pubmed:abstractText | To clinically characterize and genetically analyze members of six families who reside in the same village and manifest a rare form of retinal degeneration. | lld:pubmed |
| pubmed-article:17724221 | pubmed:language | eng | lld:pubmed |
| pubmed-article:17724221 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:17724221 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:17724221 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:17724221 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:17724221 | pubmed:issn | 0146-0404 | lld:pubmed |
| pubmed-article:17724221 | pubmed:author | pubmed-author:SharonDrorD | lld:pubmed |
| pubmed-article:17724221 | pubmed:author | pubmed-author:BaninEyalE | lld:pubmed |
| pubmed-article:17724221 | pubmed:author | pubmed-author:ObolenskyAlex... | lld:pubmed |
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| pubmed-article:17724221 | pubmed:author | pubmed-author:RosenmannAdaA | lld:pubmed |
| pubmed-article:17724221 | pubmed:author | pubmed-author:Mizrahi-Meiss... | lld:pubmed |
| pubmed-article:17724221 | pubmed:author | pubmed-author:Beit-Ya'acovA... | lld:pubmed |
| pubmed-article:17724221 | pubmed:author | pubmed-author:LandauCarmitC | lld:pubmed |
| pubmed-article:17724221 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:17724221 | pubmed:volume | 48 | lld:pubmed |
| pubmed-article:17724221 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:17724221 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:17724221 | pubmed:pagination | 4308-14 | lld:pubmed |
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| pubmed-article:17724221 | pubmed:meshHeading | pubmed-meshheading:17724221... | lld:pubmed |
| pubmed-article:17724221 | pubmed:year | 2007 | lld:pubmed |
| pubmed-article:17724221 | pubmed:articleTitle | Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease. | lld:pubmed |
| pubmed-article:17724221 | pubmed:affiliation | Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel. | lld:pubmed |
| pubmed-article:17724221 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:17724221 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:24 | entrezgene:pubmed | pubmed-article:17724221 | lld:entrezgene |
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