Associated Papers
Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the LIM2 gene in four Chinese families with congenital cataracts.
Wang X et al.
Annals of Translational Medicine, 2021
A novel mutation of LIM2 causes autosomal dominant membranous cataract in a Chinese family.
Pei R et al.
International Journal of Ophthalmology, 2020
Mutation in LIM2 Is Responsible for Autosomal Recessive Congenital Cataracts.
Irum B et al.
Plos One, 2016
Clinical and experimental advances in congenital and paediatric cataracts.
Churchill A et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences, 2011
Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.
Puk O et al.
Molecular Vision, 2011
A missense mutation in LIM2 causes autosomal recessive congenital cataract.
Ponnam SP et al.
Molecular Vision, 2008
Molecular characteristics of inherited congenital cataracts.
Huang B et al.
European Journal of Medical Genetics, 0
Select a paper to view details