Correction: Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.
- DOI
- 10.1186/s13148-026-02173-2
- Published
- 2026 Jun 13
- Container
- Clinical epigenetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s13148-026-02173-2,
title = {Correction: Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.},
author = {Koparir A and Kerkhof J and Rzasa J and Metzger E and Carbajal PB and Kolokotronis K and Koparir E and Jelting Y and Hofrichter MAH and Klepper J and König T and Runkel E and Prastyo WE and Deinlein J and Babic ND and Spiegler J and Stachelscheid N and Kunstmann E and Haaf T and Sadikovic B and Klopocki E},
year = {2026},
journal = {Clinical epigenetics},
doi = {10.1186/s13148-026-02173-2},
url = {https://doi.org/10.1186/s13148-026-02173-2}
}RIS
TY - JOUR TI - Correction: Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures. AU - Koparir A AU - Kerkhof J AU - Rzasa J AU - Metzger E AU - Carbajal PB AU - Kolokotronis K AU - Koparir E AU - Jelting Y AU - Hofrichter MAH AU - Klepper J AU - König T AU - Runkel E AU - Prastyo WE AU - Deinlein J AU - Babic ND AU - Spiegler J AU - Stachelscheid N AU - Kunstmann E AU - Haaf T AU - Sadikovic B AU - Klopocki E PY - 2026 JO - Clinical epigenetics DO - 10.1186/s13148-026-02173-2 UR - https://doi.org/10.1186/s13148-026-02173-2 ER -
APA
A, K., J, K., J, R., E, M., PB, C., K, K., E, K., Y, J., MAH, H., J, K., T, K., E, R., WE, P., J, D., ND, B., J, S., N, S., E, K., T, H., B, S., & E, K. (2026). Correction: Chromatinopathies: clinically overlapping disorders, revealing novel variants and their DNA methylation signatures.. Clinical epigenetics. https://doi.org/10.1186/s13148-026-02173-2
Source records
- pubmed · retrieved 2026-09-26T06:32:07.637Z