A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease

1. Martín-Sierra, C.
2. Requena, T.
3. Frejo, L.
4. Price, S.D.
5. Gallego-Martinez, A.
6. Batuecas-Caletrio, A.
7. Santos-Pérez, S.
8. Soto-Varela, A.
9. Lysakowski, A.
10. Lopez-Escamez, J.A.