Persistent URL of this record https://hdl.handle.net/1887/3279600
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Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss
- All authors
- Bassani, S.; Beelen, E. van; Rossel, M.; Voisin, N.; Morgan, A.; Arribat, Y.; Chatron, N.; Chrast, J.; Cocca, M.; Delprat, B.; Faletra, F.; Giannuzzi, G.; Guex, N.; Machavoine, R.; Pradervand, S.; Smits, J.J.; Kamp, J.M. van de; Ziegler, A.; Amati, F.; Marlin, S.; Kremer, H.; Locher, H.; Maurice, T.; Gasparini, P.; Girotto, G.; Reymond, A.
- Date
- 2021-10-01
- Journal
- Human Molecular Genetics
- Volume
- 30
- Issue
- 19
- Pages
- 1785 - 1796