A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia.
| Autor: | De Mingo Alemany, María Carmen, Mifsud Grau, Luis, Moreno Macián, Francisca, Ferrer Lorente, Belén, León Cariñena, Sara |
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| Zdroj: | Channels (19336950); Dec2020, Vol. 14 Issue 1, p175-180, 6p |
| Databáze: | Complementary Index |
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