Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference48 articles.
1. Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosa
2. Usher syndrome: Definition and estimate of prevalence from two high-risk populations
3. USHER SYNDROME: From Genetics to Pathogenesis
4. Molecular basis of human Usher syndrome: Deciphering the meshes of the Usher protein network provides insights into the pathomechanisms of the Usher disease
5. Mutation of a Gene Encoding a Protein with Extracellular Matrix Motifs in Usher Syndrome Type IIa
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