Identification of five novel mutations in the long isoform of the USH2A gene in Chinese families with Usher syndrome type II

Ítems similars

• 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.
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• Mutation analysis in the long isoform of USH2A in American patients with Usher Syndrome type II
  per: Yan, Denise, et al.
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• Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II
  per: Aller, E, et al.
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• Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families.
  per: Xiu-Feng Huang, et al.
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• Targeted Exome Sequencing Identified Novel USH2A Mutations in Usher Syndrome Families
  per: Huang, Xiu-Feng, et al.
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