Portaro, S., Altamura, C., Licata, N., Camerino, G. M., Imbrici, P., Musumeci, O., . . . Desaphy, J. (2015). Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita. Neuromolecular Med.
Citação norma ChicagoPortaro, Simona, et al. "Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families With Recessive Myotonia Congenita." Neuromolecular Med 2015.
Citação norma MLAPortaro, Simona, et al. "Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families With Recessive Myotonia Congenita." Neuromolecular Med 2015.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.