Cite

    Claire Bar et al.. “Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.” Human mutation, vol. 41, no. 1, 2020, pp. 69–80. http://access.bl.uk/ark:/81055/vdc_100131508417.0x000035