l carnitine for autism Unique acyl-carnitine profiles are potential biomarkers acquired mitochondrial disease in spectrum disorder Brain carnitine deficiency causes nonsyndromic

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Barton AR, Sherman MA, Mukamel RE, Loh P-R (2021) Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses

10.1002/ana.21600 [DOI] [PMC free article] [PubMed] [Google Scholar] Ursini F., Maiorino M

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Then bedding was exchanged only between mice of the same genotypes twice a week for the remaining 5 weeks before the beginning of treatment [due to the known differences in microbiome between APOE-TR mice (Tran et al., 2019)]