The parents of an eight-year-old schoolgirl from Livingston were devastated after being given the news that she has a debilitating progressive genetic condition inherited from them.

Methods The authors performed sequencing of known Coenzyme Q10 (CoQ10) deficiency genes in 22 patients with unexplained recessive or sporadic ataxia. Results CABC1/ADCK3 mutations were detected in ...

EngineAI’s SE01’s advanced end-to-end neural network system addressed the long-standing challenge of creating a natural, human-like gait, achieving unprecedented smoothness and energy ...

for the treatment of children and adults living with Friedreich ataxia (FA) to the U.S. Food and Drug Administration (FDA). "We are excited to have reached this important milestone in the ...