| pubmed-article:21633712 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C1861837 | lld:lifeskim |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C1744681 | lld:lifeskim |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C1418597 | lld:lifeskim |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C1442161 | lld:lifeskim |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C0678227 | lld:lifeskim |
| pubmed-article:21633712 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:21633712 | pubmed:dateCreated | 2011-6-2 | lld:pubmed |
| pubmed-article:21633712 | pubmed:abstractText | Cataracts are the most common cause of blindness worldwide. Inherited cataract is a clinically and genetically heterogeneous disease. Here we report a novel mutation in the paired-like homeodomain 3 (PITX3) gene segregating in a four generation English family with an isolated autosomal dominant posterior polar cataract. | lld:pubmed |
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| pubmed-article:21633712 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21633712 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21633712 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:21633712 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:21633712 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21633712 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:21633712 | pubmed:issn | 1090-0535 | lld:pubmed |
| pubmed-article:21633712 | pubmed:author | pubmed-author:FrancisPeter... | lld:pubmed |
| pubmed-article:21633712 | pubmed:author | pubmed-author:MooreAnthony... | lld:pubmed |
| pubmed-article:21633712 | pubmed:author | pubmed-author:BhattacharyaS... | lld:pubmed |
| pubmed-article:21633712 | pubmed:author | pubmed-author:WaseemNaushin... | lld:pubmed |
| pubmed-article:21633712 | pubmed:author | pubmed-author:BerryVanitaV | lld:pubmed |
| pubmed-article:21633712 | pubmed:author | pubmed-author:PrescottQuinc... | lld:pubmed |
| pubmed-article:21633712 | pubmed:copyrightInfo | © 2011 Molecular Vision | lld:pubmed |
| pubmed-article:21633712 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21633712 | pubmed:volume | 17 | lld:pubmed |
| pubmed-article:21633712 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21633712 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21633712 | pubmed:pagination | 1249-53 | lld:pubmed |
| pubmed-article:21633712 | pubmed:meshHeading | pubmed-meshheading:21633712... | lld:pubmed |
| pubmed-article:21633712 | pubmed:meshHeading | pubmed-meshheading:21633712... | lld:pubmed |
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| pubmed-article:21633712 | pubmed:meshHeading | pubmed-meshheading:21633712... | lld:pubmed |
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| pubmed-article:21633712 | pubmed:meshHeading | pubmed-meshheading:21633712... | lld:pubmed |
| pubmed-article:21633712 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21633712 | pubmed:articleTitle | A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract. | lld:pubmed |
| pubmed-article:21633712 | pubmed:affiliation | Department of Genetics, Institute of Ophthalmology, University College London, London, UK. v.berry@ucl.ac.uk | lld:pubmed |
| pubmed-article:21633712 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:21633712 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| entrez-gene:5309 | entrezgene:pubmed | pubmed-article:21633712 | lld:entrezgene |
| http://linkedlifedata.com/r... | entrezgene:pubmed | pubmed-article:21633712 | lld:entrezgene |
