Associated Papers
Two New Variants in FYCO1 Are Responsible for Autosomal Recessive Congenital Cataract in Iranian Population.
Shirzadeh E et al.
Cell Journal, 2022
Mutations in FYCO1 identified in families with congenital cataracts.
Iqbal H et al.
Molecular Vision, 2020
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract.
Patel N et al.
Human Genetics, 2017
Select a paper to view details