Associated Papers
Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients.
Waryah YM et al.
International Journal of Ophthalmology, 2019
Novel CYP1B1 mutations in consanguineous Pakistani families with primary congenital glaucoma.
Firasat S et al.
Molecular Vision, 2008
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