Associated Papers
Multimorbidity due to novel pathogenic variants in the WFS1/RP1/NOD2 genes: autosomal dominant congenital lamellar cataract, retinitis pigmentosa and Crohn's disease in a British family.
Berry V et al.
Bmj Open Ophthalmology, 2023
A novel WFS1 variant associated with isolated congenital cataracts.
Krutish A et al.
Cold Spring Harbor Molecular Case Studies, 2023
Genetic Analysis in a Swiss Cohort of Bilateral Congenital Cataract.
Rechsteiner D et al.
Jama Ophthalmology, 2021
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