학술논문
Functional characterization of the first missense variant in CEP78, a founder allele associated with cone-rod dystrophy, hearing loss, and reduced male fertility
Document Type
Artikel
Author
Ascari, G; Peelman, F; Farinelli, P; Rosseel, T; Lambrechts, N; Wunderlich, KA; Wagner, M; Nikopoulos, K; Martens, P; Balikova, I; Derycke, L; Holtappels, G; Krysko, O; Van Laethem, T; De Jaegere, S; Guillemyn, B; De Rycke, R; De Bleecker, J; Creytens, D; Van Dorpe, J; Gerris, J; Bachert, C; Neuhofer, C; Walraedt, S; Bischoff, A; Pedersen, LB; Klopstock, T; Rivolta, C; Leroy, BP; De Baere, E; Coppieters, F
Source
Human mutation. 41(5):998-1011
Subject
Language
English
English
English
ISSN
1098-1004