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Suleiman, J. et al. (2019). Homozygous loss‐of‐function variants of TASP1, a gene encoding an activator of the histone methyltransferases KMT2A and KMT2D, cause a syndrome of developmental delay, happy demeanor, distinctive facial features, and congenital anomalies. Human mutation. 40 (11), pp. 1985-1992. [Online].