GAD1

Publications

Chatron N et al. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. Brain. 2020;143(5):1447-1461. doi: 10.1093/brain/awaa085. PMID: 32282878

Weckhuysen S, Tajsharghi H. Reply: Rational therapy with vigabatrin and a ketogenic diet in a patient with GAD1 deficiency
PMID: 33169137 PMCID: PMC7719017 DOI: 10.1093/brain/awaa290

von Hardenberg S et al. Rational therapy with vigabatrin and a ketogenic diet in a patient with GAD1 deficiency.
Brain. 2020 Dec 5;143(11):e91. doi: 10.1093/brain/awaa289. PMID: 33146701.