#impairs — Public Fediverse posts
Live and recent posts from across the Fediverse tagged #impairs, aggregated by home.social.
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Mini-PCDH15 gene therapy rescues hearing in a mouse model of Usher syndrome type 1F
Usher Syndrome Type 1F is an inherited disease that causes profound #hearing #loss from birth and #impairs #vision from adolescence.
At Harvard Medical School and the Ohio State University, researchers have developed a “mini gene” approach that they believe could help to treat the disease. Their study, published in Nature Communications, focuses on protocadherin-15 (#PCDH15), a protein found in the inner ear receptor cells that, when mutated, gives rise to the unraveling of this syndrome.