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Estos nios heredan un gen SLC22A5 defectuoso de cada padre
[DOI] [PubMed] [Google Scholar] Verrotti A, Trotta D, Morgese G, Chiarelli F
Through the Cherab Foundation support group out of those that did blood draws the odds were much higher that a child with apraxia or autism tested borderline or low in carnitine
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