Mutation screening of the USH2A gene in retinitis pigmentosa and USHER patients in a Han Chinese population

Ítems similars

• Mutation screening in genes known to be responsible for Retinitis Pigmentosa in 98 Small Han Chinese Families
  per: Huang, Lulin, et al.
  Publicat: (2017)
• Whole exome sequencing identifies mutations of multiple genes in a Chinese cohort of 95 sporadic probands with presumptive retinitis pigmentosa
  per: Lulin Huang, et al.
  Publicat: (2018-12-01)
• Seven novel mutations in the long isoform of the USH2A gene in Chinese families with nonsyndromic retinitis pigmentosa and Usher syndrome Type II
  per: Xu, Wenjun, et al.
  Publicat: (2011)
• Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing
  per: Qu, Ling-hui, et al.
  Publicat: (2020)
• Whole exome sequencing identifies novel USH2A mutations and confirms Usher syndrome 2 diagnosis in Chinese retinitis pigmentosa patients
  per: Ng, Tsz Kin, et al.
  Publicat: (2019)