Open AccessMutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans
Author(s) -
Nicolas Grillet,
Martin Schwander,
Michael S. Hildebrand,
Anna Sczaniecka,
Anand Kolatkar,
Janice Velasco,
Jennifer Webster,
Kimia Kahrizi,
Hossein Najmabadi,
William J. Kimberling,
Dietrich A. Stephan,
Melanie Bahlo,
Tim Wiltshire,
Lisa M. Tarantino,
Peter Kühn,
Richard J. Smith,
Ulrich Müller
Publication year - 2009
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/6bz6-fx81
Subject(s) - hair cell , hearing loss , biology , function (biology) , outer hair cells , genetics , loss function , microbiology and biotechnology , mutation , cochlea , audiology , neuroscience , phenotype , medicine , gene