Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing

Παρόμοια τεκμήρια

• Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese population
  ανά: Huang, Lulin, κ.ά.
  Έκδοση: (2018)
• Novel deletions involving the USH2A gene in patients with Usher syndrome and retinitis pigmentosa
  ανά: García-García, Gema, κ.ά.
  Έκδοση: (2014)
• Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II
  ανά: Xu, Wenjun, κ.ά.
  Έκδοση: (2011)
• Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients
  ανά: Ng, Tsz Kin, κ.ά.
  Έκδοση: (2019)
• Multimodal imaging and genetic characteristics of Chinese patients with USH2A‐associated nonsyndromic retinitis pigmentosa
  ανά: Chong Chen, κ.ά.
  Έκδοση: (2020-11-01)