whirler

WhirlerGenetic mapping of the whirler mutationWHIRLER MICE: A Recessive Behavior Mutation in Linkage Group VIIIWhirler Mutant Hair Cells Have Less Severe Pathology than Shaker 2 or Double MutantsLinkage analysis of the whirler deafness gene on mouse chromosome 4.Metabolism rate, biochemical and endocrine alterations in male whirler mice.Metabolic and endocrine differences between the mutation whirler and normal female mice.Elongation of hair cell stereocilia is defective in the mouse mutant whirler.Photoreceptors in whirler mice show defective transducin translocation and are susceptible to short-term light/dark changes-induced ...Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with ...