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Abstract Pathogenic variants in one allele of the KAT6A gene encoding the histone acetyltransferase KAT6A (MOZ, MYST3) cause ArboledaTham syndrome (ARTHS), characterised by developmental delay, cognitive impairment, and autism-like behaviours
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A global retrospective study reported that a single hepatic cause of MASLD resulted in HCC in only 12% of cases, while a combination of other hepatic causes was found in 39%
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J.C.Wendl
Upset plot displaying benchmarking results of multi-modal pathway analysis between SpaMTP , MetaboAnalyst and Ingenuity PathwayAnalysis ( IPA ) packages (for the mouse brain paired MALDI and 10X Visium dataset 4 )
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