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Amedeo Smart

Independent Medical Education


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Rajeshwari M, Karthi S, Singh R, Efthymiou S, et al. Novel ALDH3A2 mutations in structural and functional domains of FALDH causing diverse clinical phenotypes in Sjogren-Larsson syndrome patients. Hum Mutat 2021;42:1015-1029.
PMID: 34082469


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