A novel SCNN1G mutation in a PHA I infant patient correlates with nephropathy.
Biochem Biophys Res Commun
; 519(2): 415-421, 2019 11 05.
Article
in En
| MEDLINE
| ID: mdl-31522814
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Pseudohypoaldosteronism
/
Epithelial Sodium Channels
/
Kidney Diseases
/
Mutation
Limits:
Animals
/
Humans
/
Infant
Language:
En
Journal:
Biochem Biophys Res Commun
Year:
2019
Type:
Article