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Identification of rare paired box 3 variant in strabismus by whole exome sequencing

10 Aug 2017

Abstract excerpt

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 exome sequencing were filtered by subsequent bioinformatics methods and the candidate mutation was verified as...

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PMID: 28861346
DOI: 10.18240/ijo.2017.08.06

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