A)Some individuals can suffer from medium-chain acyl-CoA
dehydrogenase (MCAD) deficiency. Which intermediates accumulate in
individuals with MCAD...
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Biology
A)Some individuals can suffer from medium-chain acyl-CoAdehydrogenase (MCAD) deficiency. Which intermediates accumulate inindividuals with MCAD deficiency? Can other intermediates still beoxidized and if so, why?
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A Mediumchain acylcoenzyme A dehydrogenase deficiency MCAD is an autosomal recessive inherited metabolic disorder caused by a deficiency of enzyme for metabolism of a group of fats called mediumchain fatty acids MCAD deficiency is caused by mutations in the ACADM gene that code for the enzyme mediumchain acylCoA dehydrogenase MCAD that is involved in mitochondrial fatty acid beta oxidation Stored fats are used by the cells for generation of energy when glucose levels are depleted Fats are generally stored as the long chain fats of C16 C18 series They are oxidized in two
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