USH2A
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- Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
- Searching the Second Hit in Patients with Inherited Retinal Dystrophies and Monoallelic Variants in ABCA4, USH2A and CEP290 by W
- Partial USH2A Deletions Contribute to Usher Syndrome in Denmark
- Determining the Causes of Recessive Retinal Dystrophy
- A Novel Locus for Usher Syndrome Type II, USH2B, Maps to Chromosome 3 at P23–24.2
- Unmasking Retinitis Pigmentosa Complex Cases by a Whole Genome
- Mouse Ush2a Conditional Knockout Project (CRISPR/Cas9)
- Genetics and Retinal Degeneration: Challenges in Optogenetic Therapy and Indentifying Pathogenic Variants
- Identification of Novel USH2A Mutations in Patients With
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- Target Sequencing of 307 Deafness Genes Identifies Candidate Genes Implicated in Microtia
- USH2A-Related Retinitis Pigmentosa: Staging of Disease Severity and Morpho-Functional Studies
- Mutation Analysis in the Long Isoform of USH2A in American Patients with Usher Syndrome Type II
- Exome Sequencing and Analysis of Induced Pluripotent Stem Cells
- A Detailed Clinical and Molecular Survey of Subjects with Nonsyndromic USH2A Retinopathy Reveals an Allelic Hierarchy of Disease-Causing Variants
- Gene Therapy for USH2A-Associated Retinal Dystrophy, Erwin Van Wijk, Phd
- The Genetics of Usher Syndrome
- Unravelling the Pathogenic Role and Genotype-Phenotype Correlation of the USH2A P.(Cys759phe) Variant Among Spanish Families