Cita APA

Martín-Sierra, C., Requena, T., Frejo, L., Price, S. D., Gallego-Martinez, A., Batuecas-Caletrio, A., . . . Lopez-Escamez, J. A. (2016). A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere’s disease. Hum Mol Genet.

Chicago Style Citation

Martín-Sierra, Carmen, et al. "A Novel Missense Variant in PRKCB Segregates Low-frequency Hearing Loss in an Autosomal Dominant Family With Meniere’s Disease." Hum Mol Genet 2016.

Cita MLA

Martín-Sierra, Carmen, et al. "A Novel Missense Variant in PRKCB Segregates Low-frequency Hearing Loss in an Autosomal Dominant Family With Meniere’s Disease." Hum Mol Genet 2016.