Congenital and Hereditary Cataracts: Epidemiology and Genetics
- 5 June 2020
- book chapter
- other
- Published by Springer Science and Business Media LLC
Abstract
No abstract availableKeywords
This publication has 59 references indexed in Scilit:
- Cataract-Causing Defect of a Mutant γ-Crystallin Proceeds through an Aggregation Pathway Which Bypasses Recognition by the α-Crystallin ChaperonePLOS ONE, 2012
- EPHA2 Polymorphisms and Age-Related Cataract in IndiaPLOS ONE, 2012
- Overexpression of Human γC-crystallin 5 bp Duplication Disrupts Lens Morphology in Transgenic MiceInvestigative Ophthalmology & Visual Science, 2011
- Mutations in FYCO1 Cause Autosomal-Recessive Congenital CataractsAmerican Journal of Human Genetics, 2011
- Mutations in the RNA Granule Component TDRD7 Cause Cataract and GlaucomaScience, 2011
- Activation of the unfolded protein response by a cataract-associated αA-crystallin mutationBiochemical and Biophysical Research Communications, 2010
- FYCO1 is a Rab7 effector that binds to LC3 and PI3P to mediate microtubule plus end–directed vesicle transportThe Journal of cell biology, 2010
- A Mutant Connexin50 with Enhanced Hemichannel Function Leads to Cell DeathInvestigative Ophthalmology & Visual Science, 2009
- EPHA2 Is Associated with Age-Related Cortical Cataract in Mice and HumansPLoS Genetics, 2009
- CHMP4B, a Novel Gene for Autosomal Dominant Cataracts Linked to Chromosome 20qAmerican Journal of Human Genetics, 2007