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Published online January 1, 2001 2,117 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

Possible mechanisms could be as follows: 1) Some researchers believe that increased GDH activity in the brain is the main cause of neurological impairment

Wang Y, Liu S

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Yap WS, Phan RCW, Yau WC, Heng SH (2015) Cryptanalysis of a new image alternate encryption algorithm based on chaotic map