Cortical myoclonus as a common and clinically actionable movement disorder phenotype of 22q11.2 deletion syndrome.
- DOI
- 10.1016/j.parkreldis.2026.108991
- Published
- 2026 Sep 21
- Container
- Parkinsonism & related disorders
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.parkreldis.2026.108991,
title = {Cortical myoclonus as a common and clinically actionable movement disorder phenotype of 22q11.2 deletion syndrome.},
author = {Reyes NGD and Grippe T and Lira VST and Angeloni B and Desai N and Marras C and Boot E and Yuen RKC and Lang AE and Andrade DM and Chen R and Bassett AS},
year = {2026},
journal = {Parkinsonism \& related disorders},
doi = {10.1016/j.parkreldis.2026.108991},
url = {https://doi.org/10.1016/j.parkreldis.2026.108991}
}RIS
TY - JOUR TI - Cortical myoclonus as a common and clinically actionable movement disorder phenotype of 22q11.2 deletion syndrome. AU - Reyes NGD AU - Grippe T AU - Lira VST AU - Angeloni B AU - Desai N AU - Marras C AU - Boot E AU - Yuen RKC AU - Lang AE AU - Andrade DM AU - Chen R AU - Bassett AS PY - 2026 JO - Parkinsonism & related disorders DO - 10.1016/j.parkreldis.2026.108991 UR - https://doi.org/10.1016/j.parkreldis.2026.108991 ER -
APA
NGD, R., T, G., VST, L., B, A., N, D., C, M., E, B., RKC, Y., AE, L., DM, A., R, C., & AS, B. (2026). Cortical myoclonus as a common and clinically actionable movement disorder phenotype of 22q11.2 deletion syndrome.. Parkinsonism & related disorders. https://doi.org/10.1016/j.parkreldis.2026.108991
Source records
- pubmed · retrieved 2026-09-26T00:22:08.394Z