A POLG2 Homozygous Mutation in an Autosomal Recessive Epilepsy Family Without Ophthalmoplegia
Journal of Clinical Neurology
; : 418-420, 2019.
Article
in En
| WPRIM
| ID: wpr-764323
Responsible library:
WPRO
ABSTRACT
No abstract available.
Full text:
1
Index:
WPRIM
Main subject:
Ophthalmoplegia
/
Epilepsy
Limits:
Humans
Language:
En
Journal:
Journal of Clinical Neurology
Year:
2019
Type:
Article