Grillet, N., et al. Mutations in LOXHD1, an Evolutionarily Conserved Stereociliary Protein, Disrupt Hair Cell Function in Mice and Cause Progressive Hearing Loss in Humans American Journal of Human Genetics (September 3, 2009)
- Ear model (Courtesy of Turbosquid)
- Cochlear cells SEM images (Courtesy of Müller Lab, Scripps Research Institute)
- Photograph of Heather Elledge and Martin Schwander in the Müller Lab (Scripps Research Institute)
- Photograph of Stuart Webb (L), Ulrich Müller (C), and Martin Schander (R) in the Müller Lab. The computer shows an image of hair cells in the cochlea visualized using a fluorescence microscope. (Scripps Research Institute)
This Human Bulletin was made possible by Science Education Partnership Award (SEPA) grant #1 R25 RR025057-01 from the National Center for Research Resources (NCRR), a component of the National Institutes of Health (NIH).