Whole-exome sequencing and electrophysiological study reveal a novel loss-of-function mutation of KCNA10 in epinephrine provoked long QT syndrome with familial history of sudden cardiac death.
Leg Med (Tokyo)
; 62: 102245, 2023 May.
Article
in En
| MEDLINE
| ID: mdl-36965351
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Long QT Syndrome
Type of study:
Etiology_studies
Limits:
Adult
/
Female
/
Humans
Language:
En
Journal:
Leg Med (Tokyo)
Journal subject:
JURISPRUDENCIA
Year:
2023
Document type:
Article
Affiliation country:
China
Country of publication:
Ireland