Absence of significant genetic alterations in the < em > VSX1 < /em > , < em > SOD1 < /em > , < em > TIMP3 < /em > , and < em > LOX < /em > genes in Brazilian patients with Keratoconus

CONCLUSION: There is absence of KC pathogenic related to mutations in the VSX1, SOD1, TIMP3 and LOX genes in the studied patients.PMID:34802378 | DOI:10.1080/13816810.2021.1992785

Source: Ophthalmic Genetics - November 22, 2021 Category: Opthalmology Authors: Alessandro Garcia Lopes Gild ásio Castello de Almeida Marcos Paulo Miola Ronan Marques Teixeira Francielly Camilla Bazilio Laurindo Pires Rodolfo Andrade Miani Luiz Carlos de Mattos Cinara C ássia Brandão Lilian Castiglioni Source Type: research