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Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis
Rare genetic variants in MEPE cause congenital facial paresis with stapes fixation, and are associated with otosclerosis
2018
H Valgaeren
I Schrauwen
L. Tomas-Roca
U. Altunoglu
M Wesdorp
Manou Sommen
M. Rahmouni
van Beusekom, , E.
M. J. Huentelman
E.E. Offeciers
I. Dhooghe
R Vincent
A. Huber
Van de Heyning P
D. Zanetti
de Leenheer, , E.M.R.
C. Gilissen
Cor Cremers
B. Verbist
de Brouwer, , A.P.M.
G W Padberg
H. Kremer
Van Camp G
Van Bokhoven H
Keywords:
Paresis
MEPE
Otosclerosis
Stapes fixation
genetic variants
Pathology
Medicine
Correction
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