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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Authors: Mingkai Yang, Yanfang Xiao, Chanjuan Chen, Zhou Chu, Guohong Hu
Cited by: 0

Abstract

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Fields of Study & Subjects

Genomics and Rare Diseases Genomic variations and chromosomal abnormalities Genetics and Neurodevelopmental Disorders

Publication details

Journal / source
Frontiers in Genetics
Volume
16
Pages
1769021–1769021
Publication date
8 January 2026
Language
EN