SLC13A5 Deficiency Disorder: From Genetics to Gene Therapy.
Genes (Basel)
; 13(9)2022 09 15.
Article
in En
| MEDLINE
| ID: mdl-36140822
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Symporters
/
Epilepsy
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Genes (Basel)
Year:
2022
Type:
Article
Affiliation country:
United States