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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10.
Ferda Percin E, Ploder LA, Yu JJ, Arici K, Horsford DJ, Rutherford A, Bapat B, Cox DW, Duncan AM, Kalnins VI, Kocak-Altintas A, Sowden JC, Traboulsi E, Sarfarazi M, McInnes RR. Ferda Percin E, et al. Among authors: sarfarazi m. Nat Genet. 2000 Aug;25(4):397-401. doi: 10.1038/78071. Nat Genet. 2000. PMID: 10932181
Optineurin in primary open angle glaucoma.
Sarfarazi M, Rezaie T. Sarfarazi M, et al. Ophthalmol Clin North Am. 2003 Dec;16(4):529-41. doi: 10.1016/s0896-1549(03)00061-0. Ophthalmol Clin North Am. 2003. PMID: 14740994 Review.
Adult-onset primary open-angle glaucoma caused by mutations in optineurin.
Rezaie T, Child A, Hitchings R, Brice G, Miller L, Coca-Prados M, Héon E, Krupin T, Ritch R, Kreutzer D, Crick RP, Sarfarazi M. Rezaie T, et al. Among authors: sarfarazi m. Science. 2002 Feb 8;295(5557):1077-9. doi: 10.1126/science.1066901. Science. 2002. PMID: 11834836
Common Molecular Challenges in Glaucoma.
Sarfarazi M. Sarfarazi M. J Ophthalmic Vis Res. 2015 Apr-Jun;10(2):95-7. doi: 10.4103/2008-322X.163767. J Ophthalmic Vis Res. 2015. PMID: 26425307 Free PMC article. No abstract available.
138 results