Associated Papers
Clinical report and genetic analysis of rare premature infant nephronophthisis caused by biallelic TTC21B variants.
Li Y et al.
Molecular Genetics & Genomic Medicine, 2024
An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.
Wang Z et al.
Npj Genomic Medicine, 2021
34215756 (PubMed )
Supplement: 41525_2021_219_MOESM1_ESM.pdf
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