Developmental and epileptic encephalopathy 44 due to compound heterozygous variants in the UBA5 gene: a case report.
- Resource Type
- Article
- Source
- Acta Epileptologica; 11/13/2023, Vol. 5 Issue 1, p1-8, 8p
- Subject
DIAGNOSIS of epilepsy GENETICS of epilepsy MAGNESIUM sulfate GENETIC mutation ELECTROENCEPHALOGRAPHY SEQUENCE analysis EPILEPSY DEVELOPMENTAL disabilities MAGNETIC resonance imaging TREATMENT effectiveness ROUTINE diagnostic tests EYE examination ADRENOCORTICOTROPIC hormone - Language
- ISSN
- 20969384