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A novel mutation and phenotypes in phosphodiesterase 6 deficiency.
Tsang SH, Tsui I, Chou CL, Zernant J, Haamer E, Iranmanesh R, Tosi J, Allikmets R. Tsang SH, et al. Am J Ophthalmol. 2008 Nov;146(5):780-8. doi: 10.1016/j.ajo.2008.06.017. Epub 2008 Aug 23. Am J Ophthalmol. 2008. PMID: 18723146 Free PMC article.
Autofluorescence imaging and spectral-domain optical coherence tomography in incomplete congenital stationary night blindness and comparison with retinitis pigmentosa.
Chen RW, Greenberg JP, Lazow MA, Ramachandran R, Lima LH, Hwang JC, Schubert C, Braunstein A, Allikmets R, Tsang SH. Chen RW, et al. Among authors: tsang sh. Am J Ophthalmol. 2012 Jan;153(1):143-54.e2. doi: 10.1016/j.ajo.2011.06.018. Epub 2011 Sep 13. Am J Ophthalmol. 2012. PMID: 21920492 Free PMC article.
Retinal phenotypes in patients homozygous for the G1961E mutation in the ABCA4 gene.
Burke TR, Fishman GA, Zernant J, Schubert C, Tsang SH, Smith RT, Ayyagari R, Koenekoop RK, Umfress A, Ciccarelli ML, Baldi A, Iannaccone A, Cremers FP, Klaver CC, Allikmets R. Burke TR, et al. Among authors: tsang sh. Invest Ophthalmol Vis Sci. 2012 Jul 3;53(8):4458-67. doi: 10.1167/iovs.11-9166. Invest Ophthalmol Vis Sci. 2012. PMID: 22661473 Free PMC article.
564 results