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Fibrosis markers also showed signs of improvement
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
As diabetes drugs continue to evolve, clinicians must stay informed about emerging therapies, expanded indications, and safety considerations to optimize patient outcomes
This study provides innovative methods and insights into therapeutic targets for LC-mediated regulation of energy metabolism remodeling in myocarditis
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