Research Usher syndromeGenetics and functional genomics

About this research group

This research group aims to identify genetic defects that underlie hereditary hearing impairment and to unravel the molecular pathogenesis. Identification of deafness genes provides knowledge on inner ear function. Furthermore, it will provide handles for the development of future therapy. read more (Donders Institute)

Research group leader

prof. dr. Hannie Kremer

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