Targeted disruption of Otog results in deafness and severe imbalance

Connexin 26 mutations in hereditary non-syndromic sensorineural deafness

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

Life Sciences, Genetics, Molecular Genetics +13

KCNQ4, a Novel Potassium Channel Expressed in Sensory Outer Hair Cells, Is Mutated in Dominant Deafness

Christian Kubisch, Björn C. Schroeder, Thomas Friedrich et al. · Cell · 1999 · 868 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

Qing Yin Zheng, Kenneth R. Johnson, Lawrence C. Erway · Hearing Research · 1999 · 842 citations

Health Professions, Audiology, Auditory Electrophysiology +12

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

Jia-Hui Xia, Chunyu Liu, Bei-sha Tang et al. · Nature Genetics · 1998 · 426 citations

Life Sciences, Genetics, Molecular Genetics +14

The Mouse Tectorins

P. Kevin Legan, Angela Rau, Jeff N. Keen et al. · Journal of Biological Chemistry · 1997 · 253 citations · Full text

Life Sciences, Biochemistry, Molecular Biology +13