Recurrent Benign Paroxysmal Positional Vertigo in DFNB16 Patients with Biallelic STRC Gene Deletions

Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis

(2021) Shuang Han et al.   Frontiers in Genetics

Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene

(2019) Zdeněk Čada et al.   EUROPEAN ARCHIVES OF OTO-RHINO-LARYNGOLOGY

Benign Paroxysmal Positional Vertigo (BPPV) in Children and Adolescents

(2018) Jacob R. Brodsky et al.   OTOLOGY & NEUROTOLOGY

Stereocilin gene variants associated with episodic vertigo: expansion of the DFNB16 phenotype

(2018) Carina Frykholm et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The Epidemiology of Deafness

(2018) Abraham M. Sheffield et al.   Cold Spring Harbor Perspectives in Medicine

Phenotypic Characterization of DFNB16-associated Hearing Loss

(2018) Daniela Back et al.   OTOLOGY & NEUROTOLOGY

Prevalence and diagnosis of vestibular disorders in children: A review

(2014) Federico Maria Gioacchini et al.   INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY

Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane

(2010) Elisabeth Verpy et al.   JOURNAL OF COMPARATIVE NEUROLOGY