Found: 10
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Targeted RP9 ablation and mutagenesis in mouse photoreceptor cells by CRISPR-Cas9.
- Published in:
- Scientific Reports, 2017, p. 43062, doi. 10.1038/srep43062
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- Article
SLC7A14 linked to autosomal recessive retinitis pigmentosa.
- Published in:
- Nature Communications, 2014, v. 5, n. 3, p. 3517, doi. 10.1038/ncomms4517
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- Publication type:
- Article
Front Cover.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 1, p. i, doi. 10.1111/cge.13584
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- Publication type:
- Article
Whole‐exome sequencing identified ARL2 as a novel candidate gene for MRCS (microcornea, rod‐cone dystrophy, cataract, and posterior staphyloma) syndrome.
- Published in:
- Clinical Genetics, 2019, v. 96, n. 1, p. 61, doi. 10.1111/cge.13541
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- Article
Causal effects of serum lipid biomarkers on early age-related macular degeneration using Mendelian randomization.
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- Genes & Nutrition, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s12263-023-00730-5
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- Article
Correction: A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration.
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- 2016
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- Correction Notice
A Naturally-Derived Compound Schisandrin B Enhanced Light Sensation in the pde6c Zebrafish Model of Retinal Degeneration.
- Published in:
- PLoS ONE, 2016, v. 11, n. 3, p. 1, doi. 10.1371/journal.pone.0149663
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- Article
Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.
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- Experimental & Molecular Medicine EMM, 2018, v. 50, n. 4, p. 1, doi. 10.1038/s12276-018-0079-0
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- Article
Mutation of IPO13 causes recessive ocular coloboma, microphthalmia, and cataract.
- Published in:
- Experimental & Molecular Medicine EMM, 2018, v. 50, n. 4, p. 1, doi. 10.1038/s12276-018-0079-0
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- Publication type:
- Article
Functional characterization of CEP250 variant identified in nonsyndromic retinitis pigmentosa.
- Published in:
- Human Mutation, 2019, v. 40, n. 8, p. 1039, doi. 10.1002/humu.23759
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- Article