Congenital hepatic fibrosis and related ciliopathies across the life course: current management, disease burden, and unmet needs in the era of genomic diagnosis and translational therapeutics.
- DOI
- 10.3389/fped.2026.1928268
- Published
- 2026
- Container
- Frontiers in pediatrics
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.3389/fped.2026.1928268,
title = {Congenital hepatic fibrosis and related ciliopathies across the life course: current management, disease burden, and unmet needs in the era of genomic diagnosis and translational therapeutics.},
author = {Wang A and He J and Liu K and Fu J and Chen J},
year = {2026},
journal = {Frontiers in pediatrics},
doi = {10.3389/fped.2026.1928268},
url = {https://doi.org/10.3389/fped.2026.1928268}
}RIS
TY - JOUR TI - Congenital hepatic fibrosis and related ciliopathies across the life course: current management, disease burden, and unmet needs in the era of genomic diagnosis and translational therapeutics. AU - Wang A AU - He J AU - Liu K AU - Fu J AU - Chen J PY - 2026 JO - Frontiers in pediatrics DO - 10.3389/fped.2026.1928268 UR - https://doi.org/10.3389/fped.2026.1928268 ER -
APA
A, W., J, H., K, L., J, F., & J, C. (2026). Congenital hepatic fibrosis and related ciliopathies across the life course: current management, disease burden, and unmet needs in the era of genomic diagnosis and translational therapeutics.. Frontiers in pediatrics. https://doi.org/10.3389/fped.2026.1928268
Source records
- pubmed · retrieved 2026-09-26T02:04:06.880Z