Summary: Researchers have discovered that a severe form of epileptic encephalopathy is caused by recessive loss-of-function mutations in the gene DENND5A. Source: McGill University. Researchers have linked a debilitating neurological disease in children to mutations in a gene that regulates neuronal development through control of protein movement within neuronal cells. The scientists from the MontrealContinue reading “Rare, Severe Neurological Disease Linked to Protein Trafficking Gene”