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Two novel variants in CYP1B1 gene: a major contributor of autosomal recessive primary congenital glaucoma with allelic heterogeneity in Pakistani patients.
Waryah YM, Iqbal M, Sheikh SA, Baig MA, Narsani AK, Atif M, Bhinder MA, Ur Rahman A, Memon AI, Pirzado MS, Waryah AM. Waryah YM, et al. Among authors: narsani ak. Int J Ophthalmol. 2019 Jan 18;12(1):8-15. doi: 10.18240/ijo.2019.01.02. eCollection 2019. Int J Ophthalmol. 2019. PMID: 30662834 Free PMC article.
Homozygous Variant in ARL3 Causes Autosomal Recessive Cone Rod Dystrophy.
Sheikh SA, Sisk RA, Schiavon CR, Waryah YM, Usmani MA, Steel DH, Sayer JA, Narsani AK, Hufnagel RB, Riazuddin S, Kahn RA, Waryah AM, Ahmed ZM. Sheikh SA, et al. Among authors: narsani ak. Invest Ophthalmol Vis Sci. 2019 Nov 1;60(14):4811-4819. doi: 10.1167/iovs.19-27263. Invest Ophthalmol Vis Sci. 2019. PMID: 31743939 Free PMC article.
Visual outcome of unilateral traumatic cataract.
Memon MN, Narsani AK, Nizamani NB. Memon MN, et al. Among authors: narsani ak. J Coll Physicians Surg Pak. 2012 Aug;22(8):497-500. J Coll Physicians Surg Pak. 2012. PMID: 22868014
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