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Exome Sequence Analysis of 14 Families With High Myopia
PURPOSE: To identify causal gene mutations in 14 families with autosomal dominant (AD) high myopia using exome sequencing. METHODS: Select individuals from 14 large Caucasian families with high myopia were exome sequenced. Gene variants were filtered to identify potential pathogenic changes. Sanger...
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| 發表在: | Invest Ophthalmol Vis Sci |
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| Main Authors: | , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
The Association for Research in Vision and Ophthalmology
2017
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5382835/ https://ncbi.nlm.nih.gov/pubmed/28384719 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.16-20883 |
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