DOI: 10.1055/s-00029025

Journal of Pediatric Epilepsy

References

Maeda H, Chiyonobu T, Yoshida M. , et al.
Establishment of isogenic iPSCs from an individual with SCN1A mutation mosaicism as a model for investigating neurocognitive impairment in Dravet syndrome.

J Hum Genet 2016;
61 (06) 565-569

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