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Case Reports

Peculiar fundus abnormalities and pathognomonic electrophysiological findings in a 14-month-old boy with NR2E3 mutations

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Pages 105-108 | Received 15 Jun 2012, Accepted 26 Aug 2012, Published online: 05 Oct 2012

REFERENCES

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  • Pachydaki S, Klaver C, Barbazetto I, et al. Phenotypic features of patients with NR2E3 mutations. Arch Ophthalmol 2009;127(1):71–75.
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