The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype.
- DOI
- 10.1186/s13023-019-1232-0
- Published
- 2019 Nov 12
- Container
- Orphanet journal of rare diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-019-1232-0,
title = {The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype.},
author = {Nijmeijer SCM and van den Born LI and Kievit AJA and Stepien KM and Langendonk J and Marchal JP and Roosing S and Wijburg FA and Wagenmakers MAEM},
year = {2019},
journal = {Orphanet journal of rare diseases},
doi = {10.1186/s13023-019-1232-0},
url = {https://doi.org/10.1186/s13023-019-1232-0}
}RIS
TY - JOUR TI - The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype. AU - Nijmeijer SCM AU - van den Born LI AU - Kievit AJA AU - Stepien KM AU - Langendonk J AU - Marchal JP AU - Roosing S AU - Wijburg FA AU - Wagenmakers MAEM PY - 2019 JO - Orphanet journal of rare diseases DO - 10.1186/s13023-019-1232-0 UR - https://doi.org/10.1186/s13023-019-1232-0 ER -
APA
SCM, N., LI, V. D. B., AJA, K., KM, S., J, L., JP, M., S, R., FA, W., & MAEM, W. (2019). The attenuated end of the phenotypic spectrum in MPS III: from late-onset stable cognitive impairment to a non-neuronopathic phenotype.. Orphanet journal of rare diseases. https://doi.org/10.1186/s13023-019-1232-0
Source records
- pubmed · retrieved 2026-09-26T14:31:33.454Z