A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
Am J Hypertens
; 32(8): 752-758, 2019 07 17.
Article
in En
| MEDLINE
| ID: mdl-30977777
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Potassium
/
Frameshift Mutation
/
Epithelial Sodium Channels
/
Liddle Syndrome
/
Hypertension
Type of study:
Diagnostic_studies
/
Prognostic_studies
/
Screening_studies
Limits:
Adolescent
/
Adult
/
Aged
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Am J Hypertens
Journal subject:
ANGIOLOGIA
Year:
2019
Document type:
Article
Affiliation country:
China