DNAJC12 in Monoamine Metabolism, Neurodevelopment, and Neurodegeneration
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Recent studies show that pathogenic variants in DNAJC12, a co-chaperone for monoamine synthesis, may cause mild hyperphenylalaninemia with infantile dystonia, young-onset parkinsonism, developmental delay and cognitive deficits. DNAJC12 has been included in ne... ...
