A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree

Lignende værker

• A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea
  af: Zhang, Lu, et al.
  Udgivet: (2009)
• A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family
  af: Yao, Ke, et al.
  Udgivet: (2008)
• A novel T→G splice site mutation of CRYBA1/A3 associated with autosomal dominant nuclear cataracts in a Chinese family
  af: Yang, Zhenfei, et al.
  Udgivet: (2012)
• A G→T splice site mutation of CRYBA1/A3 associated with autosomal dominant suture cataracts in a Chinese family
  af: Yang, Zhenfei, et al.
  Udgivet: (2011)
• A novel mutation in CRYAA is associated with autosomal dominant suture cataracts in a Chinese family
  af: Su, Dongmei, et al.
  Udgivet: (2012)