Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes

Lignende værker

• Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy
  af: Yang, Huiqin, et al.
  Udgivet: (2012)
• Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy
  af: Xu, Yu, et al.
  Udgivet: (2014)
• Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
  af: Poulter, James A., et al.
  Udgivet: (2010)
• Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
  af: Poulter, James A., et al.
  Udgivet: (2016)
• A start codon mutation of the TSPAN12 gene in Chinese families causes clinical heterogeneous familial exudative vitreoretinopathy
  af: Li, Wei, et al.
  Udgivet: (2019)