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Identification of novel disease gene for primary congenital glaucoma (PCG) through homozygosity mapping and next-generation sequencing.

Bulletin de la Societe belge d'ophtalmologie - 1 Jan 2011

Verdin H, De Baere E, Kestelyn P

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Share to Aryl Hydrocarbon Hydroxylases
Share to Chromosome Mapping
Share to Cytochrome P-450 CYP1B1
Share to Glaucoma, Angle-Closure

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 21560857

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