Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis
Author
Huentelman, M. J.
Valgaeren, H.
Schrauwen, I.
Tomas-Roca, L.
Wesdorp, M.
Sommen, M.
Rahmouni, M.
van Beusekom, E.
Offeciers, E.
dHooghe, I.
Vincent, R.
Huber, A.
Van de Heyning, P.
Zanetti, D.
De Leenheer, E. M. R.
Gilissen, C.
Cremers, C. W.
Verbist, B.
de Brouwer, A. P. M.
Padberg, G. W.
Kremer, H.
Van Camp, G.
van Bokhoven, H.
Altunoglu, U.
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