Overview Usher syndrome Additional information References Overview Gene (OMIM No.) MYO7A (#276903) Function of gene/protein Member of unconventional myosin family...

Overview Usher syndrome Additional information References Overview Gene (OMIM No.) USH1G (#607696) Function of gene/protein Scaffolding protein for Usher protein...

Overview Usher syndrome Additional information References Overview Gene (OMIM No.) CDH23 (#605516) Function of gene/protein Protein: Cadherin related 23 Cell...

Overview Usher syndrome Additional information References Overview Gene (OMIM No.) CIB2 (#605564) Function of gene/protein Protein: Calcium and integrin binding...

Overview Usher syndrome Additional information References Overview Gene (OMIM No.) USH1C (#605242) Function of gene/protein PDZ-domain containing protein Scaffolding protein...

Overview Usher syndrome Additional information References Overview Gene (OMIM No.) PCDH15 (#605514) Function of gene/protein Cell adhesion protein Component of...

Usher syndrome is a group of inherited disorders characterised by a combination of sensorineural hearing loss and retinitis pigmentosa.

Usher syndrome is a group of inherited disorders characterised by a combination of hearing loss and visual impairment due to retinitis pigmentosa.

RNA is involved in protein production from DNA in human cells. Mutations in DNA can be passed down to RNA, and a non-functional protein might be produced. RNA therapies target these "mistakes" in the RNA so that a normal functional protein can be produced instead.

Overview Usher syndrome Retinitis pigmentosa Additional information Multimodal imaging References Overview Gene (OMIM No.) USH2A (#608400) Function of gene/protein Large...