Exome-based RetNet panel analysis in a Belgian cohort with inherited retinal disease (IRD) expands the molecular and phenotypic spectrum of recently identified IRD genes

Van de Sompele, S; Van Schil, K; Van Cauwenbergh, C; Rosseel, T; De Jaegere, S; Van Laethem, T; Balikova, I; Leroy, BP; Coppieters, F; De Baere, E

EUROPEAN JOURNAL OF HUMAN GENETICS, 2019; 27 (): 54