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Kaur K 1
Showing records 1 to 1 | Display all abstracts from Kaur K12685 Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India
Chakrabarti S; Kaur K; Komatireddy S; Acharya M; Devi KR; Mukhopadhyay A; Mandal AK; Hasnain SE; Chandrasekhar G; Thomas R
Molecular Vision 2005; 11: 111-113
