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
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