Associated Papers
Two New Variants in FYCO1 Are Responsible for Autosomal Recessive Congenital Cataract in Iranian Population.
Shirzadeh E et al.
Cell Journal, 2022
Autosomal recessive cataract (CTRCT18) in the Yakut population isolate of Eastern Siberia: a novel founder variant in the FYCO1 gene.
Barashkov NA et al.
European Journal of Human Genetics : Ejhg, 2021
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
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