Clinical report and genetic analysis of rare premature infant nephronophthisis caused by biallelic TTC21B variants
Article in Molecular Genetics & Genomic Medicine (March 2024)
The most recent citing publications are shown below. View all 3 publications that cite this research output on Dimensions.
Biallelic variants in TTC21B as a rare cause of early‐onset arterial hypertension and tubuloglomerular kidney disease
Article in American Journal of Medical Genetics Part C Seminars in Medical Genetics (March 2022)
A case of proliferative glomerulosclerosis with compound heterozygous TTC21B mutations
Article in Clinica Chimica Acta (February 2022)