Identification of rare paired box 3 variant in strabismus by whole exome sequencing.
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DOI: 10.18240/ijo.2017.08.06
Abstract: 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… read more here.
Keywords: exome sequencing; rare paired; identification rare; whole exome ... See more keywords