@article{6a5035b7b6b944369dc335522f0ced6a,
title = "Genotype-Phenotype Correlation Study in a Large Series of Patients Carrying the p.Pro51Ser (p.P51S) Variant in COCH (DFNA9) Part II: A Prospective Cross-Sectional Study of the Vestibular Phenotype in 111 Carriers",
keywords = "Bilateral vestibulopathy, DFNA9, Human COCH protein, Progressive vestibulocochlear dysfunction, Sensorineural hearing loss, Vestibulo-ocular reflex, SENSORINEURAL HEARING-LOSS, QUALITY-OF-LIFE, VELOCITY STEP TEST, BILATERAL VESTIBULOPATHY, SEMICIRCULAR CANALS, GENE, DEAFNESS, IMPAIRMENT, MUTATION, DISORDER",
author = "JanssensdeVarebeke, {Sebastien P. F.} and Julie Moyaert and Erik Fransen and Britt Bulen and Celine Neesen and Katrien Devroye and {van de Berg}, Raymond and Pennings, {Ronald J. E.} and Vedat Topsakal and Olivier Vanderveken and {Van Camp}, Guy and {Van Rompaey}, Vincent",
year = "2021",
doi = "10.1097/AUD.0000000000001070",
language = "English",
volume = "42",
pages = "1525--1543",
journal = "Ear and Hearing",
issn = "0196-0202",
publisher = "LIPPINCOTT WILLIAMS & WILKINS",
number = "6",
}