Persistent URL of this record https://hdl.handle.net/1887/121899
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Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis
- All authors
- 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
- Date
- 2018-10-01
- Title of host publication
- European Journal of Human Genetics
- Volume
- 26
- Pages
- 67 - 68