Absence of significant genetic alterations in the VSX1, SOD1, TIMP3, and LOX genes in Brazilian patients with Keratoconus.
Alessandro Garcia LopesGildásio Castello AlmeidaMarcos Paulo MiolaRonan Marques TeixeiraFrancielly Camilla Bazilio Laurindo PiresRodolfo Andrade MianiLuiz Carlos de MattosCinara Cássia Brandão de MattosLilian CastiglioniPublished in: Ophthalmic genetics (2021)
There is absence of KC pathogenic related to mutations in the VSX1, SOD1, TIMP3 and LOX genes in the studied patients.