Detalhe da pesquisa
1.
SCN8A epileptic encephalopathy mutations display a gain-of-function phenotype and divergent sensitivity to antiepileptic drugs.
Acta Pharmacol Sin
; 43(12): 3139-3148, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-35902765
2.
Prime editing-based gene correction alleviates the hyperexcitable phenotype and seizures of a genetic epilepsy mouse model.
Acta Pharmacol Sin
; 44(11): 2342-2345, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37402996