| pubmed-article:8981701 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C0032854 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C0015576 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C2674016 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C0017337 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C0210492 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C1274040 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C0441510 | lld:lifeskim |
| pubmed-article:8981701 | lifeskim:mentions | umls-concept:C1561558 | lld:lifeskim |
| pubmed-article:8981701 | pubmed:dateCreated | 1997-3-7 | lld:pubmed |
| pubmed-article:8981701 | pubmed:abstractText | Mutations in the TIMP-3 (tissue inhibitor of metalloproteinase-3) gene can cause Sorsby's fundus dystrophy (SFD) and lead to choroidal neovascular membrane (CNV) formation. We studied a large American family of Irish Protestant descent with CNV inherited as an autosomal dominant trait, to determine the phenoptype and to learn whether a mutation was present in TIMP-3. | lld:pubmed |
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| pubmed-article:8981701 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8981701 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8981701 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8981701 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:8981701 | pubmed:language | eng | lld:pubmed |
| pubmed-article:8981701 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8981701 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:8981701 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:8981701 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:8981701 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:8981701 | pubmed:issn | 0065-9533 | lld:pubmed |
| pubmed-article:8981701 | pubmed:author | pubmed-author:BinghamEE | lld:pubmed |
| pubmed-article:8981701 | pubmed:author | pubmed-author:SievingP APA | lld:pubmed |
| pubmed-article:8981701 | pubmed:author | pubmed-author:PawarHH | lld:pubmed |
| pubmed-article:8981701 | pubmed:author | pubmed-author:BoskovichSS | lld:pubmed |
| pubmed-article:8981701 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:8981701 | pubmed:volume | 94 | lld:pubmed |
| pubmed-article:8981701 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:8981701 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:8981701 | pubmed:pagination | 275-94; discussion 295-7 | lld:pubmed |
| pubmed-article:8981701 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:8981701 | pubmed:meshHeading | pubmed-meshheading:8981701-... | lld:pubmed |
| pubmed-article:8981701 | pubmed:year | 1996 | lld:pubmed |
| pubmed-article:8981701 | pubmed:articleTitle | Sorsby's fundus dystrophy in a family with a Ser-181-CVS mutation in the TIMP-3 gene: poor outcome after laser photocoagulation. | lld:pubmed |
| pubmed-article:8981701 | pubmed:affiliation | Department of Ophthalmology, University of Michigan, Ann Arbor, USA. | lld:pubmed |
| pubmed-article:8981701 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:8981701 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
| pubmed-article:8981701 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:8981701 | lld:pubmed |
