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

Sebastien P. F. JanssensdeVarebeke*, Julie Moyaert, Erik Fransen, Britt Bulen, Celine Neesen, Katrien Devroye, Raymond van de Berg, Ronald J. E. Pennings, Vedat Topsakal, Olivier Vanderveken, Guy Van Camp, Vincent Van Rompaey

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

2 Citations (Web of Science)
Original languageEnglish
Pages (from-to)1525-1543
Number of pages19
JournalEar and Hearing
Volume42
Issue number6
DOIs
Publication statusPublished - 2021

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

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