M.A. Reddy
Department of Molecular Genetics
Institute of Ophthalmology
11-43 Bath Street
London EC1V 9EL
UK
Name/email consistency: high
- Characterization of the G91del CRYBA1/3-crystallin protein: a cause of human inherited cataract. Reddy, M.A., Bateman, O.A., Chakarova, C., Ferris, J., Berry, V., Lomas, E., Sarra, R., Smith, M.A., Moore, A.T., Bhattacharya, S.S., Slingsby, C. Hum. Mol. Genet. (2004)
- A clinical and molecular genetic study of a rare dominantly inherited syndrome (MRCS) comprising of microcornea, rod-cone dystrophy, cataract, and posterior staphyloma. Reddy, M.A., Francis, P.J., Berry, V., Bradshaw, K., Patel, R.J., Maher, E.R., Kumar, R., Bhattacharya, S.S., Moore, A.T. Br. J. Ophthalmol (2003)