Xiao, T; Kieninger, S; Weisschuh, N; Kohl, S; Ruther, K; Kroisel, P; Brockmann, T; Knappe, S; Kellner, U; Lagreze, W; Mazzola, P; Haack, T; Wissinger, B; Tonagel, F.
DNAJC30 disease-causing gene variants in a large Central European cohort of patients with inherited optic atrophy
INVEST OPHTH VIS SCI. 2022; 63(7):
[Poster]
Web of Science