Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina

Overview of attention for article published in Frontiers in Molecular Biosciences, July 2021

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New Research: Molecular and Cellular Studies Reveal Folding Defects of Human Ornithine Aminotransferase Variants Associated With Gyrate Atrophy of the Choroid and Retina https://t.co/CeAxNrIwla #MolBioSci

22 Aug 2021

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