Article PDF
References
Horwitz J, Bova MP, Ding LL, Haley DA, Stewart PL . Lens α-crystallin: function and structure. Eye 1999;13:403–408.
Quinlan RA, Sandilands A, Procter JE, Prescott AR, Hutcheson AM, Dahm R, et al. The eye lens cytoskeleton. Eye 1999;13:409–416.
Clark JI, Matsushima H, David LL, Clark JM . Lens cytoskeleton and transparency: a model. Eye 1999;13:417–424.
McAvoy JW, Chamberlain CG, de Iongh RU, Hales AM, Lovicu FJ . Lens development. Eye 1999;13:425–37.
Francis P, Berry V, Moore AT, Bhattacharya S . Lens biology, development and human cataractogenesis. Trends Genet 1999;15:191–6.
Graw J . Mouse models of congenital cataract. Eye 1999;13:438–444.
Brackenhoff R, Heskens H, Rossum M, Lubsen N, Schoenmakers J . Activation of the gamma-E-crystallin pseudogene in the human hereditary Coppock-like cataract. Hum Mol Genet 1994;3:279–83.
Litt M, Carrero-Valenzuela R, LaMorticella D, Schultz D, Mitchell T, Kramer P, et al. Autosomal dominant congenital cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2. Hum Mol Genet 1997;6:665–8.
Semina E, Ferrell R, Mintz-Hittner H, Bitoun P, Alwar W, Reiter R, et al. A novel homeobox gene PITX3 is mutated in families with autosomal dominant cataracts and ASMD. Nature Genet 1998;19:167–70.
Litt M, Kramer P, LaMorticella D, Murphey W, Lovrien E, Weleber R . Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA. Hum Mol Genet 1998;7:471–4.
Shiels A, Mackay D, Ionides A, Berry V, Moore A, Bhattacharya S . A missense mutation in the human connexin 50 gene (GJA8) underlies autosomal dominant ‘zonular pulverulent’ cataract, on chromosome lq. Am J Hum Genet 1998;62:526–32.
Mackay D, Ionides A, Kibar Z, Rouleau G, Berry V, Moore A, et al. Connexin 46 mutations in autosomal dominant congenital cataract. Am J Hum Genet 1999;64:1357–64.
Stephan D, Gillanders E, Vanderveen D, Freas-Lutz D, Wistow G, Baxevanis A, et al. Progressive juvenile-onset punctate cataract characterised by mutation of the gamma-D-crystallin gene. Proc Natl Acad Sci USA 1999;96:1008–12.
Lambert S, Drack A . Infantile cataracts. Surv Ophthalmol 1996;40:427–58.
Cassidy L, Taylor D . Congenital cataract and multisystem disorders. Eye 1999;13:464–473.
Lambert SR . Management of monocular congenital cataracts. Eye 1999;13:474–479.
Marcantonio JM, Vrensen GFJM . Cell biology of posterior capsular opacification. Eye 1999;13:484–488.
Spalton DJ . Posterior capsular opacification after cataract surgery. Eye 1999;13:489–492.
Foster A . Cataract - a global perspective: output, outcome and outlay. Eye 1999;13:449–453.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Francis, P., Moore, A. The lens. Eye 13, 393–394 (1999). https://doi.org/10.1038/eye.1999.112
Issue Date:
DOI: https://doi.org/10.1038/eye.1999.112