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

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Journal
Frontiers in Genetics
Published
2026-01-08
DOI
https://doi.org/10.3389/fgene.2025.1769021
Primary Topic
Genomics and Rare Diseases
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article
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article

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

Yanfang Xiao, Chanjuan Chen, Zhou Chu, Guohong Hu et al.
Frontiers in Genetics
Genomics and Rare Diseases
article

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

Yanfang Xiao, Chanjuan Chen, Zhou Chu, Guohong Hu, Mingkai Yang
article en

Abstract

No abstract available for this paper.
Frontiers in GeneticsVol. 16
Zhuzhou Central Hospital (CN), Hunan University of Technology (CN)
Zero hunger
Openalex Percentile: Top 93%
Genomics and Rare Diseases
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Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype — Yanfang Xiao, Chanjuan Chen, et al. · Frontiers in Genetics (2026) | TGRS Research Map | TGRS