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Mouse models for inherited monoamine neurotransmitter disorders

2 Jan 2024

Abstract excerpt

Abstract Several mouse models have been developed to study human defects of primary and secondary inherited monoamine neurotransmitter disorders (iMND). As the field continues to expand, current defects in corresponding mouse models include enzymes and a molecular co‐chaperone involved in monoamine synthesis and metabolism (PAH, TH, PITX3, AADC, DBH, MAOA, DNAJC6), tetrahydrobiopterin (BH4) cofactor synthesis and...

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PMID: 38168036
DOI: 10.1002/jimd.12710

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