Distinct neurological disorders with ATP1A3 mutations.
- DOI
- 10.1016/s1474-4422(14)70011-0
- Published
- 2014 May
- Container
- The Lancet. Neurology
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1016/s1474-4422-14-70011-0,
title = {Distinct neurological disorders with ATP1A3 mutations.},
author = {Heinzen EL and Arzimanoglou A and Brashear A and Clapcote SJ and Gurrieri F and Goldstein DB and Jóhannesson SH and Mikati MA and Neville B and Nicole S and Ozelius LJ and Poulsen H and Schyns T and Sweadner KJ and van den Maagdenberg A and Vilsen B and ATP1A3 Working Group},
year = {2014},
journal = {The Lancet. Neurology},
doi = {10.1016/s1474-4422(14)70011-0},
url = {https://doi.org/10.1016/s1474-4422(14)70011-0}
}RIS
TY - JOUR TI - Distinct neurological disorders with ATP1A3 mutations. AU - Heinzen EL AU - Arzimanoglou A AU - Brashear A AU - Clapcote SJ AU - Gurrieri F AU - Goldstein DB AU - Jóhannesson SH AU - Mikati MA AU - Neville B AU - Nicole S AU - Ozelius LJ AU - Poulsen H AU - Schyns T AU - Sweadner KJ AU - van den Maagdenberg A AU - Vilsen B AU - ATP1A3 Working Group PY - 2014 JO - The Lancet. Neurology DO - 10.1016/s1474-4422(14)70011-0 UR - https://doi.org/10.1016/s1474-4422(14)70011-0 ER -
APA
EL, H., A, A., A, B., SJ, C., F, G., DB, G., SH, J., MA, M., B, N., S, N., LJ, O., H, P., T, S., KJ, S., A, V. D. M., B, V., & Group, A. W. (2014). Distinct neurological disorders with ATP1A3 mutations.. The Lancet. Neurology. https://doi.org/10.1016/s1474-4422(14)70011-0
Source records
- pubmed · retrieved 2026-09-27T06:24:22.308Z