Cite
HARVARD Citation
Penkl, A. et al. (2022). A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy. American journal of medical genetics. 188 (3), pp. 941-947. [Online].
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Penkl, A. et al. (2022). A mutation in the neonatal isoform of SCN2A causes neonatal‐onset epilepsy. American journal of medical genetics. 188 (3), pp. 941-947. [Online].