A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease
- Martín-Sierra, C.
- Requena, T.
- Frejo, L.
- Price, S.D.
- Gallego-Martinez, A.
- Batuecas-Caletrio, A.
- Santos-Pérez, S.
- Soto-Varela, A.
- Lysakowski, A.
- Lopez-Escamez, J.A.
ISSN: 1460-2083, 0964-6906
Year of publication: 2016
Volume: 25
Issue: 16
Pages: 3407-3415
Type: Article