Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and human

Homozygosity Mapping Reveals Mutations of GRXCR1 as a Cause of Autosomal-Recessive Nonsyndromic Hearing Impairment

(2010) Margit Schraders et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The R109H Variant of Fascin-2, a Developmentally Regulated Actin Crosslinker in Hair-Cell Stereocilia, Underlies Early-Onset Hearing Loss of DBA/2J Mice

(2010) J.-B. Shin et al.   JOURNAL OF NEUROSCIENCE

Inheritance patterns of progressive hearing loss in laboratory strains of mice

(2009) Konrad Noben-Trauth et al.   BRAIN RESEARCH

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell

(2009) P. Heidrych et al.   HUMAN MOLECULAR GENETICS

Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses

(2009) Isabelle Roux et al.   HUMAN MOLECULAR GENETICS

Hair cell afferent synapses

(2008) Elisabeth Glowatzki et al.   CURRENT OPINION IN NEUROBIOLOGY

GRM7 variants confer susceptibility to age-related hearing impairment

(2008) Rick A. Friedman et al.   HUMAN MOLECULAR GENETICS

Sensorineural Deafness and Seizures in Mice Lacking Vesicular Glutamate Transporter 3

(2008) Rebecca P. Seal et al.   NEURON