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

Verdin, H; De Baere, E; Kestelyn, P

Verdin, H; De Baere, E; Kestelyn, P.

Affiliation

Verdin H; Center for Medical Genetics, Ghent University Hospital, Ghent, Belgium.

Bull Soc Belge Ophtalmol ; (317): 49-50, 2011.

Article in En | MEDLINE | ID: mdl-21560857

Subject(s)

Glaucoma, Angle-Closure/congenital; Glaucoma, Angle-Closure/genetics; Aryl Hydrocarbon Hydroxylases/genetics; Chromosome Mapping; Cytochrome P-450 CYP1B1; Humans; Polymorphism, Single Nucleotide

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Collection: 01-internacional Database: MEDLINE Main subject: Glaucoma, Angle-Closure Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Bull Soc Belge Ophtalmol Year: 2011 Type: Article Affiliation country: Belgium

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