TY  - JOUR
AU  - Martin-Sierra, Carmen
AU  - Requena, Teresa
AU  - Frejo, Lidia
AU  - Price, Steven D
AU  - Gallego-Martinez, Alvaro
AU  - Batuecas-Caletrio, Angel
AU  - Santos-Perez, Sofia
AU  - Soto-Varela, Andres
AU  - Lysakowski, Anna
AU  - Lopez-Escamez, Jose A
PY  - 2016
DO  - 10.1093/hmg/ddw183
UR  - http://hdl.handle.net/10668/10202
T2  - Human molecular genetics
AB  - Meniere's Disease (MD) is a complex disorder associated with an accumulation of endolymph in the membranous labyrinth in the inner ear. It is characterized by recurrent attacks of spontaneous vertigo associated with sensorineural hearing loss (SNHL)...
LA  - en
PB  - Oxford University Press
KW  - Ear, Inner
KW  - Meniere Disease
KW  - Organ of Corti
KW  - Protein Kinase C beta
KW  - Tinnitus
KW  - Adult
KW  - Animals
KW  - Female
KW  - Hearing Loss, Sensorineural
KW  - Humans
KW  - Male
KW  - Mutation, Missense
KW  - Pedigree
KW  - Rats
TI  - A novel missense variant in PRKCB segregates low-frequency hearing loss in an autosomal dominant family with Meniere's disease.
TY  - research article
VL  - 25
ER  -