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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