Correction: Case Report: Synergistic effects of an ASXL3 mutation and a 15q11.2 BP1-BP2 microdeletion in a severe neurodevelopmental phenotype
Mingkai Yang, Yanfang Xiao, Chanjuan Chen, Zhou Chu, Guohong Hu
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsGenomics and Rare Diseases · Genomic variations and chromosomal abnormalities · Genetics and Neurodevelopmental Disorders
Affiliation “Department of Pediatrics, Zhuzhou Central Hospital, Zhuzhou, Hunan, China” was omitted for authors Yanfang Xiao, Chanjuan Chen and Zhou Chu. This affiliation has now been added for authors Yanfang Xiao, Chanjuan Chen and Zhou Chu.
Authors Yanfang Xiao, Chanjuan Chen and Zhou Chu were erroneously assigned to affiliation “Department of Pediatrics, Zhuzhou Clinical College, Jishou University, Zhuzhou, Hunan, China”. This affiliation has now been removed for authors Yanfang Xiao, Chanjuan Chen and Zhou Chu.
The original article has been updated.