Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis

Author(s):
Valgaeren, H.; Schrauwen, I.; Tomas-Roca, L.; Altunoglu, U.; Wesdorp, M.; Sommen, M.; Rahmouni, M.; Beusekom, E. van; Huentelman, M.J.; Offeciers, E.; dHooghe, I.; Vincent, R.; Huber, A.; Heyning, P. van de; Zanetti, D.; Leenheer, E.M.R. de; Gilissen, C.; Cremers, C.W.; Verbist, B.; Brouwer, A.P.M. de; Padberg, G.W.; Kremer, H.; Camp, G. van; Bokhoven, H. van
Published
2018
Publication type
Other
Date issued
2018-10-01
Language
English
Publisher
NATURE PUBLISHING GROUP
hdl
1887/121899