학술논문
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration
Document Type
Article
Author
Han, J.H.; Calzetti, G.; Kaminska, K.; Quinodoz, M.; Wallerich, S.; Rivolta, C.; Rodenburg, K.; Roosing, S.; Hayman, T.; Sharon, D.; Banin, E.; Marra, M.; Yang, P.; Pennesi, M.E.; Allon, G.; Nagy, Z.Z.; Knézy, K.; Barboni, M.T.S.; Varsányi, B.; Szabó, V.; Li, Y.; Chen, R.; van den Born, L.I.; Ben-Yosef, T.; Koenekoop, R.K.
Source
In: Genetics in Medicine . (Genetics in Medicine, June 2024, 26(6))
Subject
Language
English
ISSN
15300366
10983600
10983600