Vetri, L., Calì, F., Vinci, M., Amato, C., Roccella, M., Granata, T., . . . Elia, M. (2020). A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy. European Journal of Medical Genetics, 63(4), . https://doi.org/10.1016/j.ejmg.2020.103848

Vetri, Luigi, et al. "A De Novo Heterozygous Mutation in KCNC2 Gene Implicated in Severe Developmental and Epileptic Encephalopathy." European Journal of Medical Genetics 63, no. 4 (2020). https://doi.org/10.1016/j.ejmg.2020.103848.

Vetri, Luigi, et al. "A De Novo Heterozygous Mutation in KCNC2 Gene Implicated in Severe Developmental and Epileptic Encephalopathy." European Journal of Medical Genetics, vol. 63, no. 4, 2020, https://doi.org/10.1016/j.ejmg.2020.103848.