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Introduction Mutations of one allele of the gene encoding the histone acetyltransferase KAT6A (monocytic leukaemia zinc finger protein [MOZ], MYST family member 3 [MYST3]) cause the autosomal dominant cognitive disorder, ArboledaTham syndrome (ARTHS

Br J Pharmacol 1992

By synthesizing existing evidence on potential associations between metabolites and neuropathology, this integrated analysis seeks to offer a preliminary framework that may help prioritize candidate therapeutic targets, provide clues for personalized intervention strategies, and inform future research aimed at improving neurological outcomes in MMAemia

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