Associated Papers
A recurrent variant in LIM2 causes an isolated congenital sutural/lamellar cataract in a Japanese family.
Berry V et al.
Ophthalmic Genetics, 2022
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 missense mutation in LIM2 causing isolated autosomal dominant congenital cataract.
Berry V et al.
Ophthalmic Genetics, 2020
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
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