학술논문
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
Document Type
Article
Author
Bassani, S.; Voisin, N.; Chatron, N.; Chrast, J.; Giannuzzi, G.; Pradervand, S.; Reymond, A.; Gasparini, P.; Girotto, G.; Van Beelen, E.; Locher, H.; Rossel, M.; Delprat, B.; Maurice, T.; Morgan, A.; Cocca, M.; Faletra, F.; Arribat, Y.; Amati, F.; Guex, N.; Machavoine, R.; Ziegler, A.; Marlin, S.; Smits, J.J.; Kremer, H.; Van De Kamp, J.M.
Source
In: Human Molecular Genetics . (Human Molecular Genetics, 1 October 2021, 30(19):1785-1796)
Subject
Language
English
ISSN
14602083
09646906
09646906