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Tag SNPs detect association of the CYP1B1 gene with primary open angle glaucoma

PURPOSE: The cytochrome p450 family 1 subfamily B (CYP1B1) gene is a well known cause of autosomal recessive primary congenital glaucoma. It has also been postulated as a modifier of disease severity in primary open angle glaucoma (POAG), particularly in juvenile onset families. However, the role of...

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書誌詳細
主要な著者: Burdon, Kathryn P., Hewitt, Alex W., Mackey, David A., Mitchell, Paul, Craig, Jamie E.
フォーマット: Artigo
言語:Inglês
出版事項: Molecular Vision 2010
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2994739/
https://ncbi.nlm.nih.gov/pubmed/21139974
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