arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs

Eitemau Tebyg

• Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
  gan: Van Schil, Kristof, et al.
  Cyhoeddwyd: (2018)
• Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
  gan: Van Schil, Kristof, et al.
  Cyhoeddwyd: (2018)
• Antisense Oligonucleotide-Based Downregulation of the G56R Pathogenic Variant Causing NR2E3-Associated Autosomal Dominant Retinitis Pigmentosa
  gan: Naessens, Sarah, et al.
  Cyhoeddwyd: (2019)
• Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families.
  gan: Caroline Van Cauwenbergh, et al.
  Cyhoeddwyd: (2017-01-01)
• Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families
  gan: Van Cauwenbergh, Caroline, et al.
  Cyhoeddwyd: (2017)