2004•Investigative Ophthalmology & Visual ScienceRequires access

USH3A mutations in patients with a prior diagnosis of Usher syndrome type I, Usher syndrome type II, and nonsyndromic recessive retinitis pigmentosa

Babak Jian Seyedahmadi, Eliot L. Berson, Thaddeus P. Dryja

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Key concepts: Usher syndrome, Retinitis pigmentosa, Medicine, Ophthalmology, Genetics, Biology, Retinal

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USH3A mutations in patients with a prior diagnosis of Usher syndrome type I, Usher syndrome type II, and nonsyndromic recessive retinitis pigmentosa — Research Paper | ScholarLens