PUBLICATION

CORRECTION: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsy

Authors
Corbett, M.A., van Eyk, C.L., Webber, D.L., Bent, S.J., Newman, M., Harper, K., Berry, J.G., Azmanov, D.N., Woodward, K.J., Gardner, A.E., Slee, J., Pérez-Jurado, L.A., MacLennan, A.H., Gecz, J.
ID
ZDB-PUB-220906-158
Date
2019
Source
NPJ genomic medicine   4: 11 (Other)
Registered Authors
Keywords
Gene expression, Neurodevelopmental disorders, Next-generation sequencing, Structural variation
MeSH Terms
none
PubMed
31231543 Full text @ NPJ Genom Med
Abstract
[This corrects the article DOI: 10.1038/s41525-018-0073-4.].
In the original published version of this Article, in the Methods section, the morpholino sequence for PDCD6IP AUGMO sequence was incorrectly stated as 5'-CCTTCTGACCGCTGCATGGTTTCTC-3'. It should have been 5'-ACGGGACAGAAATAAACGTCGCCAT-3'. This has been corrected for the HTML and PDF versions of the Article.
Errata / Notes
This article corrects ZDB-PUB-181220-7 .
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping