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10.1111/j.1432-1033.2004.04067.x 92 SharmaR.SharmaA.ChaudharyP.PearceV.VatsyayanR.SinghS

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Published online January 1, 2001 2,126 View 28 Download Abstract PDF Mitochondrial mutations are associated with a wide range of disorders (Kearns-Sayre and chronic progressive external ophthalmoplegia syndromes, Myoclonic epilepsy and ragged-red fibre disease, Mitoehondrial encephalomyopathy, lactic acidosis, and stroke-like episodes, Leighs disease ancl cerebellar ataxia plus pigmentary retinopathy syndromes), which is inherited maternally

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These reactions can make up 60% of bile metabolites in some cases