Mutations of the Gene Encoding Otogelin Are a Cause of Autosomal-Recessive Nonsyndromic Moderate Hearing Impairment

A Targeted Deletion in α-Tectorin Reveals that the Tectorial Membrane Is Required for the Gain and Timing of Cochlear Feedback

P. Kevin Legan, Victoria A. Lukashkina, Richard J. Goodyear et al. · Neuron · 2000 · 308 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21

Mirna Mustapha · Human Molecular Genetics · 1999 · 194 citations

Life Sciences, Genetics, Molecular Genetics +14

Sharpened cochlear tuning in a mouse with a genetically modified tectorial membrane

Ian J. Russell, P. Kevin Legan, Victoria A. Lukashkina et al. · Nature Neuroscience · 2007 · 176 citations · Full text

Life Sciences, Neurobiology, Neuroscience +14

Nonsyndromic recessive deafness DFNB18 and Usher syndrome type IC are allelic mutations of USHIC

Zubair M. Ahmed, Tenesha N. Smith, Saima Riazuddin et al. · Human Genetics · 2002 · 176 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans

Nicolas Grillet, Martin Schwander, Michael S. Hildebrand et al. · The American Journal of Human Genetics · 2009 · 162 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16