Expanding the clinical and genetic spectrum of biallelic MYO18B pathogenic variants in congenital myopathy.
- DOI
- 10.1016/j.nmd.2026.107420
- Published
- 2026 Sep 9
- Container
- Neuromuscular disorders : NMD
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.nmd.2026.107420,
title = {Expanding the clinical and genetic spectrum of biallelic MYO18B pathogenic variants in congenital myopathy.},
author = {Zaharieva IT and Donkervoort S and Longman C and Maroofian R and Foley AR and Horrocks I and Farrugia ME and Phadke R and Aguti S and McCauley J and Neuhaus SB and Essid M and Younes TB and Klaa H and Benrhouma H and Lee RHC and BenYoussef-Turki I and Kraoua I and Jamshidi Y and Chao KR and Zaki MS and Houlden H and Sarkozy A and Bönnemann CG and Muntoni F},
year = {2026},
journal = {Neuromuscular disorders : NMD},
doi = {10.1016/j.nmd.2026.107420},
url = {https://doi.org/10.1016/j.nmd.2026.107420}
}RIS
TY - JOUR TI - Expanding the clinical and genetic spectrum of biallelic MYO18B pathogenic variants in congenital myopathy. AU - Zaharieva IT AU - Donkervoort S AU - Longman C AU - Maroofian R AU - Foley AR AU - Horrocks I AU - Farrugia ME AU - Phadke R AU - Aguti S AU - McCauley J AU - Neuhaus SB AU - Essid M AU - Younes TB AU - Klaa H AU - Benrhouma H AU - Lee RHC AU - BenYoussef-Turki I AU - Kraoua I AU - Jamshidi Y AU - Chao KR AU - Zaki MS AU - Houlden H AU - Sarkozy A AU - Bönnemann CG AU - Muntoni F PY - 2026 JO - Neuromuscular disorders : NMD DO - 10.1016/j.nmd.2026.107420 UR - https://doi.org/10.1016/j.nmd.2026.107420 ER -
APA
IT, Z., S, D., C, L., R, M., AR, F., I, H., ME, F., R, P., S, A., J, M., SB, N., M, E., TB, Y., H, K., H, B., RHC, L., I, B., I, K., Y, J., KR, C., MS, Z., H, H., A, S., CG, B., & F, M. (2026). Expanding the clinical and genetic spectrum of biallelic MYO18B pathogenic variants in congenital myopathy.. Neuromuscular disorders : NMD. https://doi.org/10.1016/j.nmd.2026.107420
Source records
- pubmed · retrieved 2026-09-25T07:06:29.337Z