EurekAlert! -
26 Oct 2017 06:00
(University of Pennsylvania School of Medicine) Researchers found mutations in a master-switch protein called Epithelial Splicing Regulatory Protein 1 in individuals with a type of congenital hearing loss. In general, what connects most of the unexplained hearing-loss cases is that protein building in the cochlea during development goes awry. The cochlea has the all-important job of transforming mechanical energy in the form of sound waves into electrical signals that run along auditory nerves t...
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