Novel PRPF31 mutations associated with Chinese autosomal dominant retinitis pigmentosa patients

Gelijkaardige items

• Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa
  door: Cao, Li, et al.
  Gepubliceerd in: (2020)
• Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa
  door: Mordes, Daniel, et al.
  Gepubliceerd in: (2007)
• Targeted exome capture and sequencing identifies novel PRPF31 mutations in autosomal dominant retinitis pigmentosa in Chinese families
  door: Yang, Liping, et al.
  Gepubliceerd in: (2013)
• A Novel PRPF31 Mutation in a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa and Macular Degeneration
  door: Lu, Fang, et al.
  Gepubliceerd in: (2013)
• A novel mutation in PRPF31, causative of autosomal dominant retinitis pigmentosa, using the BGISEQ-500 sequencer
  door: Zheng, Yu, et al.
  Gepubliceerd in: (2018)