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Trends Biotechnol 35(10):937953

Later on, the molecular genetic basis of the disease was linked to a transition mutation in the snca gene A53T which results in the substitution of alanine to threonine in the N terminal 53rd amino acid of the protein leading to its abnormal aggregation (fibrillation) (Lee and Trojanowski, 2006)

Micronutrients such as vitamins, minerals and trace elements are responsible for many metabolic processes such as cell renewal, metabolism and maintaining organ function