De novo DNM1L mutation associated with mitochondrial epilepsy syndrome with fever sensitivity.
Neurol Genet
; 4(4): e258, 2018 Aug.
Article
in En
| MEDLINE
| ID: mdl-30109270
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Diagnostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Neurol Genet
Year:
2018
Document type:
Article