McClenaghan Lab Study uncovers crucial insights in Ultra-Rare Genetic Syndrome Tied to Potassium Channel Dysfunction
McClenaghan Lab Novel loss-of-function variants expand ABCC9-related intellectual disability and myopathy syndrome
McClenaghan Lab Conor McClenaghan awarded Human Frontiers Science Program Early Career Research Grant
McClenaghan Lab Bridging Personal and Population in Excitability Diseases: Will Studies of Rare Diseases Bring Generalizable Mechanisms From Monogenic Channelopathies?
