» Articles » PMID: 31048695

Author Correction: CHD3 Helicase Domain Mutations Cause a Neurodevelopmental Syndrome with Macrocephaly and Impaired Speech and Language

Abstract

The HTML and PDF versions of this Article were updated after publication to remove images of one individual from Figure 1.

Citing Articles

The complex etiology of autism spectrum disorder due to missense mutations of CHD8.

Shiraishi T, Katayama Y, Nishiyama M, Shoji H, Miyakawa T, Mizoo T Mol Psychiatry. 2024; 29(7):2145-2160.

PMID: 38438524 DOI: 10.1038/s41380-024-02491-y.


Gatad2b, associated with the neurodevelopmental syndrome GAND, plays a critical role in neurodevelopment and cortical patterning.

Abad C, Robayo M, Muniz-Moreno M, Bernardi M, Otero M, Kosanovic C Transl Psychiatry. 2024; 14(1):33.

PMID: 38238293 PMC: 10796954. DOI: 10.1038/s41398-023-02678-x.


A rigorous genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disorders.

Ben-Mahmoud A, Jun K, Gupta V, Shastri P, de la Fuente A, Park Y Front Mol Neurosci. 2022; 15:979061.

PMID: 36277487 PMC: 9582330. DOI: 10.3389/fnmol.2022.979061.