Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy.
- DOI
- 10.1016/j.ymgmr.2020.100646
- Published
- 2020 Dec
- Container
- Molecular genetics and metabolism reports
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.ymgmr.2020.100646,
title = {Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy.},
author = {Noman K and Hendriksz CJ and Radcliffe G and Roncaroli F and Moreea S and Hussain A and Stepien KM},
year = {2020},
journal = {Molecular genetics and metabolism reports},
doi = {10.1016/j.ymgmr.2020.100646},
url = {https://doi.org/10.1016/j.ymgmr.2020.100646}
}RIS
TY - JOUR TI - Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy. AU - Noman K AU - Hendriksz CJ AU - Radcliffe G AU - Roncaroli F AU - Moreea S AU - Hussain A AU - Stepien KM PY - 2020 JO - Molecular genetics and metabolism reports DO - 10.1016/j.ymgmr.2020.100646 UR - https://doi.org/10.1016/j.ymgmr.2020.100646 ER -
APA
K, N., CJ, H., G, R., F, R., S, M., A, H., & KM, S. (2020). Clinical outcomes in an adult patient with mannose phosphate isomerase-congenital disorder of glycosylation who discontinued mannose therapy.. Molecular genetics and metabolism reports. https://doi.org/10.1016/j.ymgmr.2020.100646
Source records
- pubmed · retrieved 2026-09-26T20:48:22.166Z