Novel Genetic Variants Expand the Functional, Molecular, and Pathological Diversity of KCNA1 Channelopathy.
Int J Mol Sci
; 24(10)2023 May 16.
Article
in En
| MEDLINE
| ID: mdl-37240170
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Myokymia
/
Epilepsy
/
Channelopathies
Type of study:
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
Int J Mol Sci
Year:
2023
Document type:
Article
Affiliation country:
Estados Unidos
Country of publication:
Suiza