Table 1 of
Chakrabarti, Mol Vis 2005;
11:111-113.
Table 1. Distribution of myocilin mutation Gln48His among the Indian glaucoma patients
In addition to the data presented below, Sripriya et al. [5] reported a Gln48His mutation in two Indian POAG patients out of 100 screened for defects in MYOC.
Number of Number of Gln48His Phenotype individuals mutations --------- ----------- --------- POAG 200 4 (2.0%) PCG 200 5 (2.5%) Normal 300 0 |