Congenital long QT syndrome: a case report of LQT2 and LQT13 in a neonate.
Europace
; 16(12): 1807, 2014 Dec.
Article
in En
| MEDLINE
| ID: mdl-25417227
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Long QT Syndrome
/
Genetic Predisposition to Disease
/
Polymorphism, Single Nucleotide
/
Electrocardiography
/
G Protein-Coupled Inwardly-Rectifying Potassium Channels
/
Ether-A-Go-Go Potassium Channels
Limits:
Female
/
Humans
/
Newborn
Language:
En
Journal:
Europace
Journal subject:
CARDIOLOGIA
/
FISIOLOGIA
Year:
2014
Document type:
Article
Affiliation country:
United States
Country of publication:
United kingdom