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Summary Vol.81 Issue
5 / 2018
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Arq. Bras. Oftalmol. 2018; 81 (5):
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1259
Exfoliation syndrome associated with LOXL1 gene polymorphisms in a Black patient from Latin America: a case report
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How to cite this article:
Síndrome de esfoliação associada a polimorfismos do gene LOXL1 em paciente negro da América Latina: relato de caso. Arq. Bras. Oftalmol. 2018;81(5):.
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