Global ETD Search
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Showing 1 to 1 of 1 for “"Usher Syndrom"”.
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Modeling human Usher syndrome during Drosophila melanogaster development
Human Usher syndrome is a severe and congenital form of syndromic deafness that affects 1 person in 25,000 people in the world population. Normally the stereocilia, microvillar protrusions of the apical membrane of inner ear hair cells, are organized into coherent bundles. This precise organization …