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Amedeo Smart
Independent Medical Education
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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