Partial USH2A deletions contribute to Usher syndrome in Denmark

Lignende værker

• Partial USH2A deletions contribute to Usher syndrome in Denmark
  af: Dad, Shzeena, et al.
  Udgivet: (2015)
• Usher syndrome in Denmark: mutation spectrum and some clinical observations
  af: Dad, Shzeena, et al.
  Udgivet: (2016)
• Cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangement
  af: Constantia Aristidou, et al.
  Udgivet: (2018-06-01)
• Cryptic breakpoint identified by whole-genome mate-pair sequencing in a rare paternally inherited complex chromosomal rearrangement
  af: Aristidou, Constantia, et al.
  Udgivet: (2018)
• A Common Ancestral Origin of the Frequent and Widespread 2299delG USH2A Mutation
  af: Dreyer, Bo, et al.
  Udgivet: (2001)