| pubmed-article:20144242 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:20144242 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
| pubmed-article:20144242 | lifeskim:mentions | umls-concept:C0544008 | lld:lifeskim |
| pubmed-article:20144242 | lifeskim:mentions | umls-concept:C0796344 | lld:lifeskim |
| pubmed-article:20144242 | lifeskim:mentions | umls-concept:C0021201 | lld:lifeskim |
| pubmed-article:20144242 | pubmed:dateCreated | 2010-3-9 | lld:pubmed |
| pubmed-article:20144242 | pubmed:abstractText | Mutations in COL8A2 gene which encodes the collagen alpha-2 (VIII) chain have been identified in both familial and sporadic cases of Fuchs endothelial corneal dystrophy (FECD). Heterozygous mutations in the SLC4A11 gene are also known to cause late-onset FECD. Therefore we screened for COL8A2, SLC4A11 gene variants in Indian FECD patients. | lld:pubmed |
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| pubmed-article:20144242 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:20144242 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:20144242 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:20144242 | pubmed:issn | 1471-2415 | lld:pubmed |
| pubmed-article:20144242 | pubmed:author | pubmed-author:SrinivasanMut... | lld:pubmed |
| pubmed-article:20144242 | pubmed:author | pubmed-author:SundaresanPer... | lld:pubmed |
| pubmed-article:20144242 | pubmed:author | pubmed-author:PrajnaNamperu... | lld:pubmed |
| pubmed-article:20144242 | pubmed:author | pubmed-author:HemadeviBoomi... | lld:pubmed |
| pubmed-article:20144242 | pubmed:author | pubmed-author:ArunkumarJamb... | lld:pubmed |
| pubmed-article:20144242 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:20144242 | pubmed:volume | 10 | lld:pubmed |
| pubmed-article:20144242 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:20144242 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:20144242 | pubmed:pagination | 3 | lld:pubmed |
| pubmed-article:20144242 | pubmed:dateRevised | 2010-9-28 | lld:pubmed |
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| pubmed-article:20144242 | pubmed:year | 2010 | lld:pubmed |
| pubmed-article:20144242 | pubmed:articleTitle | Genetic analysis of patients with Fuchs endothelial corneal dystrophy in India. | lld:pubmed |
| pubmed-article:20144242 | pubmed:affiliation | Department of Genetics, Dr G Venkataswamy Eye Research Institute, Aravind Medical Research Foundation, #1 Anna nagar, Madurai, Tamilnadu, India. | lld:pubmed |
| pubmed-article:20144242 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:20144242 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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