The γS-Crystallin Gene Is Mutated in Autosomal Recessive Cataract in Mouse

This publication has 22 references indexed in Scilit:

• Missense mutations in MIP underlie autosomal dominant ‘polymorphic’ and lamellar cataracts linked to 12q
  Nature Genetics, 2000
• Lens biology: development and human cataractogenesis
  Trends in Genetics, 1999
• Connexin46 Mutations in Autosomal Dominant Congenital Cataract
  American Journal of Human Genetics, 1999
• A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD
  Nature Genetics, 1998
• INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes Clearer
  American Journal of Human Genetics, 1998
• A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q
  American Journal of Human Genetics, 1998
• Infantile cataracts
  Survey of Ophthalmology, 1996
• Mutations in the founder of the MIP gene family underlie cataract development in the mouse
  Nature Genetics, 1996
• Primary structure of βs-crystallin from human lens
  Biochemical Journal, 1992
• Structure of the bovine eye lens γs-crystallin gene (formerly βs)
  Gene, 1989