Discovering the missing 'LINC' to deafness
Tel Aviv — Because half of all instances of hearing loss are linked to genetic mutations, advanced gene research is an invaluable tool for uncovering causes of deafness — and one of the biggest hopes for the development of new therapies. Now Prof. Karen Avraham of the Sackler Faculty of Medicine at Tel Aviv University has discovered a significant mutation in a LINC family protein — part of the cells of the inner ear — that could lead to new treatments for hearing disorders.
Her team of researchers, including Dr. Henning Horn and Profs. Colin Stewart and Brian Burke of ...






