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A novel mutation in transforming growth factor-beta induced protein (TGFβIp) reveals secondary structure perturbation in lattice corneal dystrophy.
Lakshminarayanan R, Vithana EN, Chai SM, Chaurasia SS, Saraswathi P, Venkatraman A, Rojare C, Venkataraman D, Tan D, Aung T, Beuerman RW, Mehta JS. Lakshminarayanan R, et al. Among authors: chai sm. Br J Ophthalmol. 2011 Oct;95(10):1457-62. doi: 10.1136/bjophthalmol-2011-300651. Epub 2011 Aug 10. Br J Ophthalmol. 2011. PMID: 21835759
Retinal vasculopathy in Fanconi anemia.
Chai SM, Mathur R, Ong SG. Chai SM, et al. Ophthalmic Surg Lasers Imaging. 2009 Sep-Oct;40(5):498-500. doi: 10.3928/15428877-20090901-11. Ophthalmic Surg Lasers Imaging. 2009. PMID: 19772276
Clinical and genetic aspects of the TGFBI-associated corneal dystrophies.
Lakshminarayanan R, Chaurasia SS, Anandalakshmi V, Chai SM, Murugan E, Vithana EN, Beuerman RW, Mehta JS. Lakshminarayanan R, et al. Among authors: chai sm. Ocul Surf. 2014 Oct;12(4):234-51. doi: 10.1016/j.jtos.2013.12.002. Epub 2014 Jul 18. Ocul Surf. 2014. PMID: 25284770 Review.
37 results