VPS13A is a lipid transfer protein localized at different membrane contact sites between organelles,1, 2, 3, 4, 5, 6 and mutations in the corresponding gene produce a rare neurodegenerative disease called chorea‐acanthocytosis (ChAc), also known as VPS13A disease.7, 8, 9. Here, VPS13A is linked to neurodegenerative disease.