Dominant Leber congenital amaurosis, cone-rod degeneration, and retinitis pigmentosa caused by mutant versions of the transcription factor CRX
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Reference46 articles.
1. Recommendations for a nomenclature system for human gene mutations
2. Temporal and spatial expression patterns of the CRX transcription factor and its downstream targets. Critical differences during human and mouse eye development.
3. Functional Domains of the Cone-Rod Homeobox (CRX) Transcription Factor
4. Crx, a Novel Otx-like Paired-Homeodomain Protein, Binds to and Transactivates Photoreceptor Cell-Specific Genes
5. Mutational analysis and clinical correlation in Leber congenital amaurosis
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