An MIP/AQP0 mutation with impaired trafficking and function underlies an autosomal dominant congenital lamellar cataract

Ítems similars

• A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract
  per: Arora, A, et al.
  Publicat: (2006)
• The E368Q Mutant Allele of GJA8 is Associated with Congenital Cataracts with Intrafamilial Variation in a South Indian Family
  per: Senthil Kumar, G, et al.
  Publicat: (2016)
• Novel Single-Base Deletional Mutation in Major Intrinsic Protein (MIP) in Autosomal Dominant Cataract
  per: Geyer, David D., et al.
  Publicat: (2006)
• A Novel αB-Crystallin Mutation Associated with Autosomal Dominant Congenital Lamellar Cataract
  per: Liu, Yizhi, et al.
  Publicat: (2006)
• A novel MIP gene mutation associated with autosomal dominant congenital cataracts in a Chinese family
  per: Yu, Yibo, et al.
  Publicat: (2014)