Biallelic variants in TTC21B as a rare cause of early-onset arterial hypertension and tubuloglomerular kidney disease.
Am J Med Genet C Semin Med Genet
; 190(1): 109-120, 2022 03.
Article
in En
| MEDLINE
| ID: mdl-35289079
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Glomerulosclerosis, Focal Segmental
/
Hypertension
/
Kidney Diseases
Type of study:
Prognostic_studies
/
Systematic_reviews
Limits:
Female
/
Humans
/
Male
Language:
En
Journal:
Am J Med Genet C Semin Med Genet
Journal subject:
GENETICA MEDICA
Year:
2022
Type:
Article
Affiliation country:
United kingdom