Recurrent SLC1A2 variants cause epilepsy via a dominant negative mechanism

Andrew B Stergachis1, Jonai Pujol-Giménez2,3, Gergely Gyimesi2,3

  • 1Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Boston, MA.

Annals of Neurology
|April 3, 2019
PubMed

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