A case of mucopolysaccharidosis I with severely increased albuminuria and Graves’ disease, and functional analysis of previously uncharacterized variant
- DOI
- 10.1186/s13023-026-04527-8
- Published
- 2026-08-07
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04527-8,
title = {A case of mucopolysaccharidosis I with severely increased albuminuria and Graves’ disease, and functional analysis of previously uncharacterized variant},
author = {Kun Dong and Junran J. Peng and Xue Zhou and Qiusha Zhu and Changhong Li and Yan Yang},
year = {2026},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-026-04527-8},
url = {https://doi.org/10.1186/s13023-026-04527-8}
}RIS
TY - JOUR TI - A case of mucopolysaccharidosis I with severely increased albuminuria and Graves’ disease, and functional analysis of previously uncharacterized variant AU - Kun Dong AU - Junran J. Peng AU - Xue Zhou AU - Qiusha Zhu AU - Changhong Li AU - Yan Yang PY - 2026 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-026-04527-8 UR - https://doi.org/10.1186/s13023-026-04527-8 ER -
APA
Dong, K., Peng, J. J., Zhou, X., Zhu, Q., Li, C., & Yang, Y. (2026). A case of mucopolysaccharidosis I with severely increased albuminuria and Graves’ disease, and functional analysis of previously uncharacterized variant. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-026-04527-8
Source records
- crossref · retrieved 2026-11-10T13:06:17.202Z