1. A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia. Issue 1 (1st January 2020) Authors: De Mingo Alemany, María Carmen; Mifsud Grau, Luis; Moreno Macián, Francisca; Ferrer Lorente, Belén; León Cariñena, Sara Journal: Channels Issue: Volume 14:Issue 1(2020) Page Start: 175 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗