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Role of MYH9 in Hearing and Deafness

Anil K. Lalwani M.D.
Mendik Foundation Professor of Otolaryngology and Chairman and Professor of Physiology and Neuroscience

Departments of Otolaryngology and Physiology and Neuroscience

Member of NYU Otolaryngology Associates

 
Research Summary
We have recently identified MYH9, a non muscle heavy chain myosin, as the gene responsible for DFNA17 (autosomal dominant hearing impairment). Currently, we are assessing the consequences of specific MYH9 mutations on protein function, its contribution to human deafness, and are utilizing knock-out and knock-in transgenic mouse models to assess its role in normal hearing.
 
Research Information
Research Interests Molecular genetics of deafness
Gene therapy for deafness
Research Keywords genetics, molecular biology, deafness, gene therapy
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