Congenital, Hereditary, and Neonatal Diseases and Abnormalities: News and Research on Eye Diseases, Hereditary

MeSH tree: C16.320.290

Researcher builds new model to examine Usher syndrome

Usher syndrome, a rare inherited genetic disease, is a leading cause of combined deafness and blindness with type 2A (USH2A) being the most common form. USH2A, caused by mutations in the USH2A gene, can include hearing loss ...

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