A novel mutation KCNQ1p.Thr312del is responsible for long QT syndrome type 1.
Heart Vessels
; 34(1): 177-188, 2019 Jan.
Article
in En
| MEDLINE
| ID: mdl-30008122
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
DNA
/
Romano-Ward Syndrome
/
KCNQ1 Potassium Channel
/
Mutation
Type of study:
Prognostic_studies
Limits:
Child, preschool
/
Humans
/
Male
Language:
En
Journal:
Heart Vessels
Journal subject:
CARDIOLOGIA
Year:
2019
Document type:
Article
Affiliation country:
China
Country of publication:
Japan