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
Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.
Puk O et al.
Molecular Vision, 2011
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