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
Case report: ZFYVE19 gene mutation is associated with familial cholestasis.
Xue MY et al.
Frontiers in Medicine, 2024
Combining Panel-Based Next-Generation Sequencing and Exome Sequencing for Genetic Liver Diseases.
Chen CB et al.
The Journal of Pediatrics, 2023
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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