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pro vyhledávání: '"Gladys Villalobos Alonso"'
Publikováno v:
Journal of Ophthalmology, Iss 2, Pp 63-64 (2023)
Gyrus atrophy is a rare autosomal recessive hereditary disease secondary to a mutation of the OAT gene on chromosome 10 which results in a deficiency of the mitochondrial enzyme ornithine aminotransferase that causes a 20-fold increase in serum conce
Externí odkaz:
https://doaj.org/article/6e317e18470b4b63bf431c95e825f17b
