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Glutathione Synthetase Deficiency as a Cause of Hereditary Hemolytic Disease New England Journal of Medicine GLUTATHIONE SYNTHESIS PMC Laboratory diagnosis of biotinidase deficiency, 2017 update: a technical standard and guideline of the American College of Medical Genetics and Genomics Genetics in Medicine Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations Genetics in Medicine

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Your body typically absorbs vitamins and minerals slowly, as they have to pass through your digestive system and break down

B12 is a water soluble vitamin that can exist in a number of forms, all of which contain the mineral cobalt

Prevalence of chronic kidney disease in China: Results from the Sixth China Chronic Disease and Risk Factor Surveillance

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