Imbrici, P., Altamura, C., Camerino, G. M., Mangiatordi, G. F., Conte, E., Maggi, L., . . . Camerino, D. C. (2016). Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: A paradigm to understand and treat ion channelopathies. FASEB J.
Style de citation ChicagoImbrici, Paola, et al. "Multidisciplinary Study of a New ClC-1 Mutation Causing Myotonia Congenita: A Paradigm to Understand and Treat Ion Channelopathies." FASEB J 2016.
Style de citation MLAImbrici, Paola, et al. "Multidisciplinary Study of a New ClC-1 Mutation Causing Myotonia Congenita: A Paradigm to Understand and Treat Ion Channelopathies." FASEB J 2016.
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