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Insights into the mechanisms of sterol transport between organelles.
Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death.
Publication: Slower Piezo1 inactivation in dehydrated hereditary stomatocytosis (xerocytosis).
Team: Pathophysiology of Na+ channels and neuronal excitability
Team: MOLECULAR and INTEGRATIVE MECHANOBIOLOGY
Fabrice DUPRAT
Sophie DEMOLOMBE
Eric HONORE