ロード中...
Exome sequencing study of 20 patients with high myopia
BACKGROUND: High myopia is a common ocular disease worldwide. To expand our current understanding of the genetic basis of high myopia, we carried out a whole exome sequencing (WES) study to identify potential causal gene mutations. METHODS: A total of 20 individuals with high myopia were exome seque...
保存先:
| 出版年: | PeerJ |
|---|---|
| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
PeerJ Inc.
2018
|
| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6148412/ https://ncbi.nlm.nih.gov/pubmed/30245926 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7717/peerj.5552 |
| タグ: |
タグ追加
タグなし, このレコードへの初めてのタグを付けませんか!
|