Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
Kiyoto Kurima(National Institute on Deafness and Other Communication Disorders), Linda Peters(National Institute on Deafness and Other Communication Disorders), Yandan Yang(National Institute on Deafness and Other Communication Disorders), Saima Riazuddin(National Institute on Deafness and Other Communication Disorders), Zubair M. Ahmed(Centre of Excellence in Molecular Biology), Sadaf Naz(National Institute on Deafness and Other Communication Disorders), Deidre Arnaud(Louisiana State University Health Sciences Center New Orleans), Stacy S. Drury(Louisiana State University Health Sciences Center New Orleans), Jianhong Mo(National Institutes of Health), Tomoko Makishima(National Institute on Deafness and Other Communication Disorders), Manju Ghosh(All India Institute of Medical Sciences), P.S.N. Menon(All India Institute of Medical Sciences), Dilip Deshmukh, Carole Oddoux(New York University), Harry Ostrer(New York University), S.G. Khan(Centre of Excellence in Molecular Biology), Sheikh Riazuddin(Centre of Excellence in Molecular Biology), Prescott L. Deininger(Tulane University), Lori L. Hampton(National Institute of Neurological Disorders and Stroke), Susan L. Sullivan(National Institute on Deafness and Other Communication Disorders), James F. Battey(National Institute of Neurological Disorders and Stroke), Bronya J.B. Keats(Louisiana State University Health Sciences Center New Orleans), Edward R. Wilcox(National Institutes of Health), Thomas B. Friedman(National Institutes of Health), Andrew J. Griffith(National Institute on Deafness and Other Communication Disorders)
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