DNM1 encephalopathy − atypical phenotype with hypomyelination due to a novel de novo variant in the DNM1 gene

Autor: Kolnikova, Miriam, Skopkova, Martina, Ilencikova, Denisa, Foltan, Tomas, Payerova, Jaroslava, Danis, Daniel, Klimes, Iwar, Stanik, Juraj, Gasperikova, Daniela
Zdroj: In Seizure: European Journal of Epilepsy March 2018 56:31-33
Databáze: ScienceDirect