Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.
- DOI
- 10.1038/s41431-026-02219-2
- Published
- 2026 Nov
- Container
- European journal of human genetics : EJHG
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1038/s41431-026-02219-2,
title = {Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.},
author = {Komatsu K and Sugie A and Nitta Y and Osaka J and Mansoor Hussain UH and Kubota M and Shimozawa N and Carter MT and Zwijnenburg PJG and Waisfisz Q and Boschann F and Horn D and Nakashima M and Saitsu H},
year = {2026},
journal = {European journal of human genetics : EJHG},
doi = {10.1038/s41431-026-02219-2},
url = {https://doi.org/10.1038/s41431-026-02219-2}
}RIS
TY - JOUR TI - Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder. AU - Komatsu K AU - Sugie A AU - Nitta Y AU - Osaka J AU - Mansoor Hussain UH AU - Kubota M AU - Shimozawa N AU - Carter MT AU - Zwijnenburg PJG AU - Waisfisz Q AU - Boschann F AU - Horn D AU - Nakashima M AU - Saitsu H PY - 2026 JO - European journal of human genetics : EJHG DO - 10.1038/s41431-026-02219-2 UR - https://doi.org/10.1038/s41431-026-02219-2 ER -
APA
K, K., A, S., Y, N., J, O., UH, M. H., M, K., N, S., MT, C., PJG, Z., Q, W., F, B., D, H., M, N., & H, S. (2026). Correction: Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder.. European journal of human genetics : EJHG. https://doi.org/10.1038/s41431-026-02219-2
Source records
- pubmed · retrieved 2026-11-10T13:44:41.488Z