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Inoltre, lacetil-L-carnitina un eccellente trasportatore fisiologico di acidi grassi , che favorisce laccelerazione del metabolismo
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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Retrieved 31 January 2012
Circ Res 2020

Menna Thomas Menten John S
