Correction: Case Report: Synergistic effects of an <i>ASXL3</i> mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype.

Yang M, Xiao Y, Chen C, Chu Z, Hu G.

Open source

DOI: 10.3389/fgene.2025.1769021
Published: 2026-01-09
Container: Front Genet
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.3389/fgene.2025.1769021,
  title = {Correction: Case Report: Synergistic effects of an \&lt;i\&gt;ASXL3\&lt;/i\&gt; mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype.},
  author = {Yang M and  Xiao Y and  Chen C and  Chu Z and  Hu G.},
  year = {2025},
  journal = {Front Genet},
  doi = {10.3389/fgene.2025.1769021},
  url = {https://doi.org/10.3389/fgene.2025.1769021}
}

RIS

TY  - JOUR
TI  - Correction: Case Report: Synergistic effects of an &lt;i&gt;ASXL3&lt;/i&gt; mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype.
AU  - Yang M
AU  -  Xiao Y
AU  -  Chen C
AU  -  Chu Z
AU  -  Hu G.
PY  - 2025
JO  - Front Genet
DO  - 10.3389/fgene.2025.1769021
UR  - https://doi.org/10.3389/fgene.2025.1769021
ER  -

APA

M, Y., Y, X., C, C., Z, C., & G., H. (2025). Correction: Case Report: Synergistic effects of an <i>ASXL3</i> mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype.. Front Genet. https://doi.org/10.3389/fgene.2025.1769021

Source records

europe-pmc · retrieved 2026-09-26T00:36:30.325Z
doaj · retrieved 2026-09-26T00:36:30.347Z

Correction: Case Report: Synergistic effects of an &lt;i&gt;ASXL3&lt;/i&gt; mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype.

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Cite this work

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APA

Source records

Correction: Case Report: Synergistic effects of an <i>ASXL3</i> mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype.