Site Logo
  1. Home
  2. Past Issues
  3. Summary Vol.81 Issue 5 / 2018
  4. Article

Article

Send this article by email

Cartas

Síndrome de esfoliação associada a polimorfismos do gene LOXL1 em paciente negro da América Latina: relato de caso

Submission is temporarily unavailable. reCAPTCHA validation has not been configured yet.
Read in Portuguese Print PDF English
Open Access
Share

How to cite this article:

Takitani GES, Azevedo AGB, Motta FL, Teixeira SH, Sallum JMF, Vessani RM. Síndrome de esfoliação associada a polimorfismos do gene LOXL1 em paciente negro da América Latina: relato de caso. Arq. Bras. Oftalmol. 2018;81(5):437-439. 10.5935/0004-2749.20180084
Export citation