BMC Medicine · 2023 · 29 citations · 41 references
ZDHHC21 p.T209S is a novel, candidate causal gene mutation in a Chinese FAD pedigree. Our discoveries strongly suggest that aberrant protein palmitoylation mediated by ZDHHC21 mutations is a new pathogenic mechanism of AD, warranting further investigations for the development of therapeutic interventions.
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Mutation of the mouse klotho gene leads to a syndrome resembling ageing.
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