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A 5-year-old girl with decreased vision in the left eye
Digital Journal of Ophthalmology 2015
Volume 21, Number 2
May 9, 2015
DOI: 10.5693/djo.03.2014.09.001
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Joel Yap, MBChB | Department of Ophthalmology, Greenlane Clinical Centre, Auckland District Health Board, New Zealand
Dianne Sharp, FRANZCO | Department of Ophthalmology, Greenlane Clinical Centre, Auckland District Health Board, New Zealand
Shuan Dai, FRANZCO | Department of Ophthalmology, Greenlane Clinical Centre, Auckland District Health Board, New Zealand
References
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2. Subash M, Rotsos T, Wright GA, et al. Unilateral vitelliform maculopathy: a comprehensive phenotype study with molecular screening of BEST1 and PRPH2. Br J Ophthalmol 2012;96:719-22.
3. Cascavilla ML, Quergues G, Stenirri S, Battaglia Parodi M, Quergues L, Bandello F. Unilateral vitelliform phenotype in autosomal recessive bestophinopathy. Ophthalmic Res 2012;48:146-50.
4. Burgess R, Millar I, Leroy B, Urquhart J, Fearon I, Baere E, Brown P, Robson A, Wright G, Kestelyn P, Holder G, Webster A, Mandon F and Black G. Biallelic mutation BEST1 causes a distinct retinopathy in humans. Am J Hum Genet 2008; 82:19-31.
5. Zhang Q, Small K and Grossniklaus H. Clinicopathological findings in Best vitelliform macular dystrophy. Graefes Arch Clin Exp Ophthalmol 2011;249:745-51.
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