Use of patient derived urine renal epithelial cells to confirm pathogenicity of PKHD1 alleles
Elisa Molinari; Shalabh Srivastava; Rebecca M. Dewhurst; John A. Sayer · 2020 · BMC Nephrology
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
Abstract Background PKHD1 is the main genetic cause of autosomal recessive polycystic kidney disease (ARPKD), a hereditary hepato-renal fibrocystic disorder which is the most important cause of end-stage renal disease during early…
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Metadata source: Crossref · DOI 10.1186/s12882-020-02094-z