Autism spectrum disorder early in development associated with CHD8 mutations among two Chinese children
Abstract Background Autism spectrum disorder (ASD) is a heterogeneous group of neurodevelopmental disorders. Genetically based subtype identification may prove more beneficial not only in illuminating the course and prognosis, but also for individualized treatment targets of an ASD sub-group. Increa...
Main Authors: | Jiangping Wang, Jinling Liu, Yi Gao, Kaixuan Wang, Kewen Jiang |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2018-10-01
|
Series: | BMC Pediatrics |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s12887-018-1307-4 |
Similar Items
-
CHD7 missense variants and clinical characteristics of Chinese males with infertility
by: Leilei Li, et al.
Published: (2020-09-01) -
Genetic Variability of the Functional Domains of Chromodomains Helicase DNA-Binding (CHD) Proteins
by: Ana R. Cardoso, et al.
Published: (2021-11-01) -
Clinical Study of 8 Cases of CHD2 Gene Mutation–Related Neurological Diseases and Their Mechanisms
by: Xiaona Luo, et al.
Published: (2022-03-01) -
The epigenetic factor CHD4 contributes to metastasis by regulating the EZH2/β-catenin axis and acts as a therapeutic target in ovarian cancer
by: Jieyu Wang, et al.
Published: (2023-01-01) -
From X-inactivation to neurodevelopment: CHD8-transcription factors (TFs) competitive binding at regulatory regions of CHD8 target genes can contribute to correct neuronal differentiation
by: Andrea Cerase, et al.
Published: (2023-01-01)