Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference58 articles.
1. Molecular genetics of retinitis pigmentosa
2. Identification of genes causing photoreceptor degenerations leading to blindness
3. Rhodopsin mutations in inherited retinal dystrophies and dysfunctions
4. Inborn errors of signal transduction: Mutations in G proteins and G protein-coupled receptors as a cause of disease
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