INVITED EDITORIAL The Genetics of Cataract: Our Vision Becomes Clearer

This publication has 53 references indexed in Scilit:

• Marner's cataract (CAM) assigned to chromosome 16: linkage to haptoglobin
  Clinical Genetics, 2008
• A Missense Mutation in the Human Connexin50 Gene (GJA8) Underlies Autosomal Dominant “Zonular Pulverulent” Cataract, on Chromosome 1q
  American Journal of Human Genetics, 1998
• Disruption of α3 Connexin Gene Leads to Proteolysis and Cataractogenesis in Mice
  Cell, 1997
• A New Locus for Dominant “Zonular Pulverulent” Cataract, on Chromosome 13
  American Journal of Human Genetics, 1997
• Cataract Mutations as a Tool for Developmental Geneticists
  Ophthalmic Research, 1996
• Activation of the ΓE-crystallin pseudogene in the human hereditary Coppock-like cataract
  Human Molecular Genetics, 1994
• A frameshift mutation in the γE–crystallin gene of the Elo mouse
  Nature Genetics, 1992
• GENETIC RISK ASSESSMENT
  Annual Review of Genetics, 1991
• Overexpression of the vimentin gene in transgenic mice inhibits normal lens cell differentiation.
  The Journal of cell biology, 1989
• Confirmation of genetic heterogeneity in autosomal dominant forms of congenital cataracts from linkage studies
  Cytogenetic and Genome Research, 1978