Cite
HARVARD Citation
De Mingo Alemany, M. et al. (2020). A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia. Channels. 14 (1), pp. 175-180. [Online].
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De Mingo Alemany, M. et al. (2020). A de novo CACNA1D missense mutation in a patient with congenital hyperinsulinism, primary hyperaldosteronism and hypotonia. Channels. 14 (1), pp. 175-180. [Online].