Noncoding mutation in RPGRIP1 contributes to inherited retinal degenerations

Zou, G; Zhang, T; Cheng, XS; Igelman, AD; Wang, J; Qian, XY; Fu, SY; Wang, KQ; Koenekoop, RK; Fishman, GA; Yang, P; Li, YM; Pennesi, ME; Chen, R

Chen, R (corresponding author), Baylor Coll Med, Human Genome Sequencing Ctr, Room N1519,One Baylor Plaza, Houston, TX 77030 USA.

MOLECULAR VISION, 2021; 27 (): 95

Abstract

Purpose: Despite the extensive use of next-generation sequencing (NGS) technology to identify disease-causing genomic variations, a major gap in our u......

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