Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants.
HGG Adv
; 3(4): 100131, 2022 Oct 13.
Article
in En
| MEDLINE
| ID: mdl-36035247
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
HGG Adv
Year:
2022
Document type:
Article