Persistent URL of this record https://hdl.handle.net/1887/119504
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De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment
- All authors
- Smits, J.J.; Oostrik, J.; Beynon, A.J.; Kant, S.G.; Gans, P.A.M.D.; Rotteveel, L.J.C.; Wassink-Ruiter, J.S.K.; Free, R.H.; Maas, S.M.; Kamp, J. van de; Merkus, P.; Koole, W.; Feenstra, I.; Admiraal, R.J.C.; Lanting, C.P.; Schraders, M.; Yntema, H.G.; Pennings, R.J.E.; Kremer, H.; DOOFNL Consortium
- Date
- 2019-01-31
- Journal
- Human Genetics
- Volume
- 138
- Issue
- 1
- Pages
- 61 - 72