Ontology highlight
ABSTRACT:
SUBMITTER: Isgrig K
PROVIDER: S-EPMC5363211 | biostudies-literature | 2017 Mar
REPOSITORIES: biostudies-literature
Isgrig Kevin K Shteamer Jack W JW Belyantseva Inna A IA Drummond Meghan C MC Fitzgerald Tracy S TS Vijayakumar Sarath S Jones Sherri M SM Griffith Andrew J AJ Friedman Thomas B TB Cunningham Lisa L LL Chien Wade W WW
Molecular therapy : the journal of the American Society of Gene Therapy 20170221 3
Dizziness and hearing loss are among the most common disabilities. Many forms of hereditary balance and hearing disorders are caused by abnormal development of stereocilia, mechanosensory organelles on the apical surface of hair cells in the inner ear. The deaf whirler mouse, a model of human Usher syndrome (manifested by hearing loss, dizziness, and blindness), has a recessive mutation in the whirlin gene, which renders hair cell stereocilia short and dysfunctional. In this study, wild-type whi ...[more]