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 |
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Zdroj: | In Seizure: European Journal of Epilepsy March 2018 56:31-33 |
Databáze: | ScienceDirect |
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