Related Experiment Video

Updated: May 12, 2026

A High-Throughput Luciferase Assay to Evaluate Proteolysis of the Single-Turnover Protease PCSK9
08:14

A High-Throughput Luciferase Assay to Evaluate Proteolysis of the Single-Turnover Protease PCSK9

Published on: August 28, 2018

Expanding the genotypic spectrum of PCSK1 deficiency: A novel mutation in severe neonatal diarrhea

Eleonora Saraceno1, Angelo Corso Faini2, Silvia Deaglio2

  • 1Department of Public Health and Pediatrics Postgraduate School of Pediatrics, Regina Margherita Children Hospital, University of Turin Turin Italy.

JPGN Reports
|May 11, 2026
PubMed

Keywords:
PCSK1 mutationcongenital diarrheaendocrinopathygenomic testing

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