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

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

Fulltext

XML

Search on Google

Full text: Available Index: IMSEAR (South-East Asia) Main subject: Female / Humans / Male / DNA Mutational Analysis / Molecular Sequence Data / Aryl Hydrocarbon Hydroxylases / Base Sequence / Glycoproteins / Glaucoma, Open-Angle / Age of Onset Type of study: Etiology study Country/Region as subject: Asia Language: English Journal: J Genet Year: 2008 Type: Article

Similar

MEDLINE

LILACS

LIS

Fulltext

XML

Search on Google