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Identification of rare paired box 3 variant in strabismus by whole exome sequencing
AIM: To identify the potentially pathogenic gene variants that contributes to the etiology of strabismus. METHODS: A Chinese pedigree with strabismus was collected and the exomes of two affected individuals were sequenced using the next-generation sequencing technology. The resulting variants from e...
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| Yayımlandı: | Int J Ophthalmol |
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| Asıl Yazarlar: | , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
International Journal of Ophthalmology Press
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5554839/ https://ncbi.nlm.nih.gov/pubmed/28861346 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18240/ijo.2017.08.06 |
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