Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

David P. Kelsell, John Dunlop, Howard P. Stevens et al. · Nature · 1997 · 1.5K citations

Mendelian Disorder, Developmental Biology, Genetic Disorder +2

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw et al. · Human Molecular Genetics · 1997 · 635 citations · Full text

Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus

Elisabeth Verpy, Saber Masmoudi, Ingrid Zwaenepoel et al. · Nature Genetics · 2001 · 191 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

Targeted disruption of Otog results in deafness and severe imbalance

Marie‐Christine Simmler, Martine Cohen‐Salmon, A. Amraoui et al. · Nature Genetics · 2000 · 147 citations

Allergy, Audiology, Otog Results +5

Mutations in OTOGL , Encoding the Inner Ear Protein Otogelin-like, Cause Moderate Sensorineural Hearing Loss

Kemal O. Yariz, Duygu Duman, Celia Zazo Seco et al. · The American Journal of Human Genetics · 2012 · 127 citations · Full text

Developmental Biology, Genetics, Audiology +10