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Mutations in the gene encoding OCTN2, SLC22A5 , can impair fatty acid metabolism and lead to systemic primary carnitine deficiency (SPCD, OMIM 212140) 8 , an autosomal recessive disorder whose clinical manifestations include cardiomyopathy, hypoglycemia, chronic muscle weakness and liver dysfunction 9

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Hypothyroidism has also been associated with insulin resistance and risk of type 2 diabetes

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aurata (SAM-2 and SAF-1) presents a good source of that key amino acid with the best umami taste among examined fish roe

The most commonly reported issues are gastrointestinal, including nausea, diarrhea, vomiting, constipation, and stomach pain