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

Những quyển sách tương tự

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