Mitochondrial diseases are primarily genetic disorders that are essential for encoding proteins involved in mitochondrial function and generating energy as ATP through oxidative phosphorylation (OXPHOS). This causes mitochondrial dysfunction and energy deficits in the cell, affecting organs and tissues with… Continue Reading →

A Breakthrough in Huntington’s Disease Gene therapy trials in the UK led by professors Sarah Tabrizi and Ed Wild have givenhope to the thousands of people with Huntington’s disease. Until now, this devastating diseasehas been incurable. It is an autosomal… Continue Reading →