De novo and inherited loss-of-function variants of ATP2B2 are associated with rapidly progressive hearing impairment

Author(s):
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
Published
2019
Publication type
Article / Letter to editor
Date issued
2019-01-31
Language
English
Is part of
Human Genetics (2019), Vol. 138, no. 1, p. 61-72
hdl
1887/119504
doi
10.1007/s00439-018-1965-1