Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy

Samankaltaisia teoksia

• Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy
  Tekijä: Fei, Ping, et al.
  Julkaistu: (2015)
• Identification of two novel LRP5 mutations in families with familial exudative vitreoretinopathy
  Tekijä: Fei, Ping, et al.
  Julkaistu: (2014)
• A start codon mutation of the TSPAN12 gene in Chinese families causes clinical heterogeneous familial exudative vitreoretinopathy
  Tekijä: Li, Wei, et al.
  Julkaistu: (2019)
• Novel TSPAN12 mutations in patients with familial exudative vitreoretinopathy and their associated phenotypes
  Tekijä: Yang, Huiqin, et al.
  Julkaistu: (2011)
• Mutations in TSPAN12 Cause Autosomal-Dominant Familial Exudative Vitreoretinopathy
  Tekijä: Poulter, James A., et al.
  Julkaistu: (2010)