DNM1L-related encephalopathy in infancy with Leigh syndrome-like phenotype and suppression-burst.
Clin Genet
; 90(5): 472-474, 2016 11.
Article
in En
| MEDLINE
| ID: mdl-27301544
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Brain Diseases
/
Leigh Disease
/
Mitochondrial Proteins
/
GTP Phosphohydrolases
/
Microtubule-Associated Proteins
Limits:
Humans
Language:
En
Journal:
Clin Genet
Year:
2016
Document type:
Article