Associated Papers
Mutations of CYP1B1 and FOXC1 genes for childhood glaucoma in Japanese individuals.
Fuse N et al.
Japanese Journal of Ophthalmology, 2024
Somatic Mutations within Myocilin due to Aging May Be a Potential Risk Factor for Glaucoma.
Sazhnyev Y et al.
Genes, 2024
38397193 (PubMed )
Supplement: genes-15-00203-s001.zip › genes-2821445-supplementary.xlsx › Sheet1
Structure‒function‒pathogenicity analysis of C-terminal myocilin missense variants based on experiments and 3D models.
Zhou B et al.
Frontiers in Genetics, 2022
36267417 (PubMed )
Supplement: Table3.xlsx › Sheet1
Common and rare myocilin variants: Predicting glaucoma pathogenicity based on genetics, clinical, and laboratory misfolding data.
Scelsi HF et al.
Human Mutation, 2021
Identification and functional characterization of a novel MYOC mutation in two primary open angle glaucoma families from The Netherlands.
Hogewind BF et al.
Molecular Vision, 2007
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