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
The use of autozygosity mapping and next-generation sequencing in understanding anterior segment defects caused by an abnormal development of the lens.
Gillespie RL et al.
Human Heredity, 2014
Mutations in FYCO1 cause autosomal-recessive congenital cataracts.
Chen J et al.
American Journal of Human Genetics, 2011
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