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De novo FZR1 loss-of-function variants cause developmental and epileptic encephalopathies.
Brain. 2022 Jun 3;145(5):1684-1697. doi: 10.1093/brain/awab409.
Brain. 2022.
PMID: 34788397
Free PMC article.
The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome.
Larsen J, Johannesen KM, Ek J, Tang S, Marini C, Blichfeldt S, Kibaek M, von Spiczak S, Weckhuysen S, Frangu M, Neubauer BA, Uldall P, Striano P, Zara F; MAE working group of EuroEPINOMICS RES Consortium; Kleiss R, Simpson M, Muhle H, Nikanorova M, Jepsen B, Tommerup N, Stephani U, Guerrini R, Duno M, Hjalgrim H, Pal D, Helbig I, Møller RS.
Larsen J, et al.
Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
Epilepsia. 2015.
PMID: 26537434
Free article.
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