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To prevent a recurrence, avoid foods that have triggered past episodes

SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) (1517), an autosomal recessive disorder characterized by skeletal myopathy, progressive cardiomyopathy, hypoglycemia, and hyperammonemia

Each easy-to-swallow softgel delivers 100mcg of highly bioavailable vitamin K2 as menaquinone-7 (MK-7), naturally sourced from natto, a traditional Japanese fermented soybean product

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