Clinical and genetic spectrum of dual rare genetic diseases revealed by whole-exome sequencing in 14 pediatric patients.
- DOI
- 10.1186/s13023-026-04462-8
- Published
- 2026-09-21
- Container
- Orphanet J Rare Dis
- 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:10.1186/s13023-026-04462-8,
title = {Clinical and genetic spectrum of dual rare genetic diseases revealed by whole-exome sequencing in 14 pediatric patients.},
author = {Zhao M and Li F and Lu X and Zheng H and Du X.},
year = {2026},
journal = {Orphanet J Rare Dis},
doi = {10.1186/s13023-026-04462-8},
url = {https://doi.org/10.1186/s13023-026-04462-8}
}RIS
TY - JOUR TI - Clinical and genetic spectrum of dual rare genetic diseases revealed by whole-exome sequencing in 14 pediatric patients. AU - Zhao M AU - Li F AU - Lu X AU - Zheng H AU - Du X. PY - 2026 JO - Orphanet J Rare Dis DO - 10.1186/s13023-026-04462-8 UR - https://doi.org/10.1186/s13023-026-04462-8 ER -
APA
M, Z., F, L., X, L., H, Z., & X., D. (2026). Clinical and genetic spectrum of dual rare genetic diseases revealed by whole-exome sequencing in 14 pediatric patients.. Orphanet J Rare Dis. https://doi.org/10.1186/s13023-026-04462-8
Source records
- europe-pmc · retrieved 2026-09-26T10:10:31.053Z