pubmed-article:19096718 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0030705 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C1553355 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0339573 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0220908 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0298987 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0442711 | lld:lifeskim |
pubmed-article:19096718 | lifeskim:mentions | umls-concept:C0205214 | lld:lifeskim |
pubmed-article:19096718 | pubmed:dateCreated | 2008-12-19 | lld:pubmed |
pubmed-article:19096718 | pubmed:abstractText | The gene coding cytochrome P4501B1 (CYP1B1) has been shown to be a major cause of primary congenital glaucoma in the Iranian population. More recently it was shown to also be important in juvenile-onset open angle glaucoma (JOAG). We aimed to further investigate the role of CYP1B1 in a larger cohort of primary open angle glaucoma (POAG) patients which included late-onset patients. We also aimed to set up a microarray based protocol for mutation screening with an intent of using the protocol in a future population level screening program. | lld:pubmed |
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pubmed-article:19096718 | pubmed:language | eng | lld:pubmed |
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pubmed-article:19096718 | pubmed:citationSubset | IM | lld:pubmed |
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pubmed-article:19096718 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:19096718 | pubmed:issn | 1090-0535 | lld:pubmed |
pubmed-article:19096718 | pubmed:author | pubmed-author:NBB | lld:pubmed |
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pubmed-article:19096718 | pubmed:author | pubmed-author:BayatBehnazB | lld:pubmed |
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pubmed-article:19096718 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:19096718 | pubmed:volume | 14 | lld:pubmed |
pubmed-article:19096718 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:19096718 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:19096718 | pubmed:pagination | 2349-56 | lld:pubmed |
pubmed-article:19096718 | pubmed:dateRevised | 2011-11-17 | lld:pubmed |
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pubmed-article:19096718 | pubmed:year | 2008 | lld:pubmed |
pubmed-article:19096718 | pubmed:articleTitle | Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol. | lld:pubmed |
pubmed-article:19096718 | pubmed:affiliation | School of Biology, University College of Science, University of Tehran, Tehran, Iran. | lld:pubmed |
pubmed-article:19096718 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:19096718 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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