Detalhe da pesquisa
1.
Genetic analysis using targeted exome sequencing of 53 Vietnamese children with developmental and epileptic encephalopathies.
Am J Med Genet A
; 188(7): 2048-2060, 2022 07.
Artigo
Inglês
| MEDLINE | ID: mdl-35365919
2.
De novo homozygous variant of the SCN1A gene in a patient with severe Dravet syndrome complicated by acute encephalopathy.
Neurogenetics
; 22(2): 133-136, 2021 05.
Artigo
Inglês
| MEDLINE | ID: mdl-33674996