DDX3X-Related Neurodevelopmental Disorder Presenting as a Cerebral Palsy Mimic
Author:
- 14 May 2026
- journal article
- Published by Elsevier in Pediatric Neurology
- Vol. 181, 38-41
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical DevelopmentNeuron, 2020
- Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt SignalingThe American Journal of Human Genetics, 2015
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular PathologyGenetics in Medicine, 2015
- Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsyMolecular Psychiatry, 2015