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CYP1B1 mutational screening in a Portuguese cohort of primary congenital glaucoma patients

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Primary congenital glaucoma (PCG) is a rare and severe autosomal recessive disease, characterized by high intraocular pressure during the neonatal or early infantile period. If undetected and timel... Click to show full abstract

Primary congenital glaucoma (PCG) is a rare and severe autosomal recessive disease, characterized by high intraocular pressure during the neonatal or early infantile period. If undetected and timel...

Keywords: congenital glaucoma; mutational screening; primary congenital; screening portuguese; cyp1b1 mutational

Journal Title: Ophthalmic Genetics
Year Published: 2017

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