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Publications by Brith Otterud

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi Arabia

American Journal of Human Genetics

English

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Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans

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A Spectrum of CYP1B1 Mutations Associated With Primary Congenital Glaucoma in Families of Pakistani Descent

Human Genome Variation

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Goniodysgenesis Variability and Activity of CYP1B1 Genotypes in Primary Congenital Glaucoma

Multidisciplinary

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CYP1B1 Mutations in French Patients With Early-Onset Primary Open-Angle Glaucoma

Journal of Medical Genetics

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Corneal Profile in Primary Congenital Glaucoma

Acta Ophthalmologica

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Newborn Primary Congenital Glaucoma

Journal of Pediatric Ophthalmology and Strabismus

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Post Occupancy Evaluation of Primary Schools in Saudi Arabia

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ACTN1 Mutations Cause Congenital Macrothrombocytopenia

American Journal of Human Genetics

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Mutations in FYCO1 Cause Autosomal-Recessive Congenital Cataracts

American Journal of Human Genetics

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