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Complex genetics of glaucoma: defects in CYP1B1, and not MYOC, cause pathogenesis in an early-onset POAG patient with double variants at both loci.

Acharya, Moulinath; Mukhopadhyay, Arijit; Bhattacharjee, Ashima; Thakur, Sanjay K D; Bandyopadhyay, Arun K; Ray, Kunal.

J Genet ; 2008 Dec; 87(3): 265-9

Article in English | IMSEAR | ID: sea-114353

Subject(s)

Adult , Age of Onset , Aryl Hydrocarbon Hydroxylases/genetics , Base Sequence , Cytoskeletal Proteins/genetics , DNA Mutational Analysis , Eye Proteins/genetics , Female , Glaucoma, Open-Angle/enzymology , Glycoproteins/genetics , Humans , India/epidemiology , Male , Molecular Sequence Data , Mutation/genetics

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