A Chinese family with progressive childhood cataracts and IVS3+1G>A CRYBA3/A1 mutations

Lignende værker

• A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family
  af: Jin, Chongfei, et al.
  Udgivet: (2012)
• A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family
  af: Wang, Wei, et al.
  Udgivet: (2010)
• Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family
  af: Yao, Ke, et al.
  Udgivet: (2011)
• 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 splice site mutation of CRYBA3/A1 gene associated with congenital cataract in a Chinese family
  af: Wu, Meng-Han, et al.
  Udgivet: (2017)