Molecular Screening ofRhodopsinandPeripherin/RDSGenes in Mexican Families with Autosomal Dominant Retinitis Pigmentosa
Author:
Publisher
Informa UK Limited
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Link
http://www.tandfonline.com/doi/pdf/10.3109/02713680903283169
Reference46 articles.
1. Retinitis Pigmentosa
2. Prevalence of Retinitis Pigmentosa in Maine
3. The epidemiology of retinitis pigmentosa in Denmark
4. Retinitis pigmentosa
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1. Variant Profiling of a Large Cohort of 138 Chinese Families With Autosomal Dominant Retinitis Pigmentosa;Frontiers in Cell and Developmental Biology;2021-02-01
2. The F220C and F45L rhodopsin mutations identified in retinitis pigmentosa patients do not cause pathology in mice;Scientific Reports;2020-05-05
3. “In situ” observation of the role of chloride ion binding to monkey green sensitive visual pigment by ATR-FTIR spectroscopy;Physical Chemistry Chemical Physics;2018
4. Identification of the genetic determinants responsible for retinal degeneration in families of Mexican descent;Ophthalmic Genetics;2017-09-25
5. Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families;PLOS ONE;2017-01-11
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