Cite
HARVARD Citation
Stergachis, A. et al. (2019). Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. Annals of neurology. 85 (6), pp. 921-926. [Online].
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Stergachis, A. et al. (2019). Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism. Annals of neurology. 85 (6), pp. 921-926. [Online].