Two rare copy number variants involving loss of NPHP1, MALL, and MTLN genes contribute to nephronophthisis-induced nephropathy progression in a family: A case report.
Niger J Clin Pract
; 26(4): 524-527, 2023 Apr.
Article
in En
| MEDLINE
| ID: mdl-37203120
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Renal Insufficiency, Chronic
/
Kidney Failure, Chronic
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Child
/
Female
/
Humans
/
Male
Language:
En
Journal:
Niger J Clin Pract
Journal subject:
MEDICINA
Year:
2023
Document type:
Article
Country of publication:
India