A novel mutation in PRPF31, causative of autosomal dominant retinitis pigmentosa, using the BGISEQ-500 sequencer

類似資料

• Novel PRPF31 mutations associated with Chinese autosomal dominant retinitis pigmentosa patients
  著者:: Xu, Fei, 等
  出版事項: (2012)
• Identification of photoreceptor genes affected by PRPF31 mutations associated with autosomal dominant retinitis pigmentosa
  著者:: Mordes, Daniel, 等
  出版事項: (2007)
• Genomic Rearrangements of the PRPF31 Gene Account for 2.5% of Autosomal Dominant Retinitis Pigmentosa
  著者:: Sullivan, Lori S., 等
  出版事項: (2006)
• Identification of two novel PRPF31 mutations in Chinese families with non‐syndromic autosomal dominant retinitis pigmentosa
  著者:: Cao, Li, 等
  出版事項: (2020)
• A Novel PRPF31 Mutation in a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa and Macular Degeneration
  著者:: Lu, Fang, 等
  出版事項: (2013)