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Association of the MYOC p.(Gln368Ter) Variant With Glaucoma in a Finnish Population
IMPORTANCE: The c.1102C>T, p.(Gln368Ter) variant in the myocilin (MYOC) gene is a known risk allele for glaucoma. It is the most common MYOC risk variant for glaucoma among individuals of European ancestry, and its prevalence is highest in Finland. Furthermore, exfoliation syndrome has high preva...
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| 出版年: | JAMA Ophthalmol |
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| 主要な著者: | , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
American Medical Association
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8176385/ https://ncbi.nlm.nih.gov/pubmed/34081096 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/jamaophthalmol.2021.1610 |
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