Gyrate Atrophy Ocular and Systemic Study (GYROS)
Description preview
1 Project Summary/Abstract for GYROS
2 Gyrate atrophy is a rare inherited chorioretinal degeneration that is associated with
3 hyperornithinemia caused by autosomal recessive mutations in the ornithine aminotransferase
4 (OAT) gene and leads to severe loss of vision. The current standard of care treatment is a
5 highly burdensome…
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