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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148412/ https://www.ncbi.nlm.nih.gov/pubmed/30245926 http://dx.doi.org/10.7717/peerj.5552 |