A recurrent PAX6 mutation is associated with aniridia and congenital progressive cataract in a Chinese family

Podobné jednotky

• Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family
  Autor: Yao, Ke, a další
  Vydáno: (2011)
• A Chinese family with progressive childhood cataracts and IVS3+1G>A CRYBA3/A1 mutations
  Autor: Zhu, Yanan, a další
  Vydáno: (2010)
• A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family
  Autor: Wang, Wei, a další
  Vydáno: (2010)
• A novel PAX6 mutation in a large Chinese family with aniridia and congenital cataract
  Autor: Cai, Fucheng, a další
  Vydáno: (2010)
• A nonsense mutation in CRYGC associated with autosomal dominant congenital nuclear cataract in a Chinese family
  Autor: Yao, Ke, a další
  Vydáno: (2008)