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OMIM: 607483) is a neurometabolic autosomal recessive disorder caused by a mutation in the SLC19A3 gene, characterized by subacute encephalopathy with confusion, convulsions, muscle rigidity, ataxia, dysarthria, and dystonia, which can be fatal if left untreated

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Consistently, they find that levels of LET-363/mTOR are decreased in glp-1

(1996) Phospholipase C 4 is involved in modulating the visual response in mice

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