Chatron, N. Et Al. 2020. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. BRAIN , vol.143 , 1447-1461.

Chatron, N., Becker, F., Morsy, H., Schmidts, M., Hardies, K., Tuysuz, B., ... Roselli, S.(2020). Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. BRAIN , vol.143, 1447-1461.

Chatron, Nicolas Et Al. "Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy," BRAIN , vol.143, 1447-1461, 2020

Chatron, Nicolas Et Al. "Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy." BRAIN , vol.143, pp.1447-1461, 2020

Chatron, N. Et Al. (2020) . "Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy." BRAIN , vol.143, pp.1447-1461.

@article{article, author={Nicolas Chatron Et Al. }, title={Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy}, journal={BRAIN}, year=2020, pages={1447-1461} }