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Amedeo Smart

Independent Medical Education


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Reynisdottir T, Anderson KJ, Boukas L, Bjornsson HT, et al. Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2. PLoS Genet 2022;18:e1010278.
PMID: 35727845


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