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

Citation
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. (2016). A novel missense variant inPRKCBsegregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease. Human Molecular Genetics, 25(16), 3407–3415. https://doi.org/10.1093/hmg/ddw183
DOI:
DOI: 10.1093/hmg/ddw183
Year of publication:
2016