A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family

Liknande verk

• A novel mutation in the major intrinsic protein (MIP) associated with autosomal dominant congenital cataracts in a Chinese family
  av: Wang, Wei, et al.
  Publicerad: (2010)
• Characterization of a novel mutation in the CRYBB2 gene associated with autosomal dominant congenital posterior subcapsular cataract in a Chinese family
  av: Yao, Ke, et al.
  Publicerad: (2011)
• A Nonsense Mutation of γD-crystallin Associated with Congenital Nuclear and Posterior Polar Cataract in a Chinese Family
  av: Zhai, Yi, et al.
  Publicerad: (2014)
• A novel mutation in the MIP gene is associated with autosomal dominant congenital nuclear cataract in a Chinese family
  av: Yang, Guoxing, et al.
  Publicerad: (2011)
• A novel GJA3 mutation causing autosomal dominant congenital perinuclear cataracts
  av: Yanan Zhu, et al.
  Publicerad: (2025-04-01)