Associated Papers
Compound heterozygous mutations in CYP1B1 gene leads to severe primary congenital glaucoma phenotype.
Song N et al.
International Journal of Ophthalmology, 2019
Cytochrome P450 1B1 gene mutations in Japanese patients with primary congenital glaucoma(1).
Kakiuchi-Matsumoto T et al.
American Journal of Ophthalmology, 2001
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