Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies. Submitted by iguillen on Mon, 06/17/2019 - 12:37 del Pozo MGonzález-, Méndez-Vidal C, Bravo-Gil N, et al. Exome sequencing reveals novel and recurrent mutations with clinical significance in inherited retinal dystrophies. PLoS One. 2014;9(12):e116176. doi:10.1371/journal.pone.0116176.