Article

Achary, M.S. and Reddy, A.B.M. and Chakrabarti, S. and Panicker, S.G. and Mandal, A.K. and Ahmed, N. and Balasubramanian, D. and Hasnain, S.E. and Nagarajaram, H.A. (2006) Disease-Causing Mutations in Proteins: Structural Analysis of the CYP1b1 Mutations Causing Primary Congenital Glaucoma in Humans. Biophysical Journal, 91 (12). pp. 4329-4339. ISSN 0006-3495

Kaur, K. and Reddy, A.B.M. and Mukhopadhyay, A. and Mandal, A.K. and Hasnain, S.E. and Ray, K. and Thomas, R. and Balasubramanian, D. and Chakrabarti, S. (2005) Myocilin gene implicated in primary congenital glaucoma. Clinical Genetics, 67 (4). pp. 335-340. ISSN 0009-9163

Chakrabarti, S. and Kaur, K. and Sreelatha, K. and Acharya, M. and Devi, K.R. and Mukhopadhyay, A. and Mandal, A.K. and Hasnain, S.E. and Chandrasekhar, G. and Thomas, R. and Ray, K. (2005) Gln48His is the prevalent myocilin mutation in primary open angle and primary congenital glaucoma phenotypes in India. Molecular Vision, 11. pp. 111-3. ISSN 1090-0535

Reddy, A.B.M. and Kaur, K. and Mandal, A.K. and Panicker, S.G. and Thomas, R. and Hasnain, S.E. and Balasubramanian, D. and Chakrabarti, S. (2004) Mutation spectrum of the CYP1B1 gene in Indian primary congenital glaucoma patients. Molecular vision, 10. pp. 696-702. ISSN 1090-0535