Publications

Export 1 results:
Author Title [ Year(Asc)]
Filters: Author is Chatron, Nicolas and Keyword is Abnormalities, Multiple  [Clear All Filters]
2020
Chatron, N. et al. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy. Brain 143, 1447-1461 (2020).