Associated Papers
Clinical features and long-term outcomes of patients with ZFYVE19 variants.
Li JQ et al.
Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver, 2025
ZFYVE19 gene mutation: A novel variant of progressive familial intrahepatic cholestasis.
Ben Sabbahia D et al.
Jpgn Reports, 2024
Non-syndromic perspective on a unique progressive familial intrahepatic cholestasis variant: ZFYVE19 mutation.
Özkeçeci CF et al.
The Turkish Journal of Pediatrics, 2024
Biallelic loss-of-function ZFYVE19 mutations are associated with congenital hepatic fibrosis, sclerosing cholangiopathy and high-GGT cholestasis.
Luan W et al.
Journal of Medical Genetics, 2021
A ZFYVE19 gene mutation associated with neonatal cholestasis and cilia dysfunction: case report with a novel pathogenic variant.
Mandato C et al.
Orphanet Journal of Rare Diseases, 2021
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