Interconnected Gene Networks Underpin the Clinical Overlap of HNRNPH1-Related and Rubinstein–Taybi Intellectual Disability Syndromes
Author:
Funder
Ministry of Health
Publisher
Frontiers Media SA
Subject
General Neuroscience
Reference23 articles.
1. Variants in HNRNPH2 on the X chromosome are associated with a neurodevelopmental disorder in females;Bain;Am. J. Hum. Genet,2016
2. Detailed clinical and psychological phenotype of the X-linked HNRNPH2-related neurodevelopmental disorder;Bain;Neurol. Genet.,2021
3. Transcriptome analysis of iPSC-derived neurons from Rubinstein–Taybi patients reveals deficits in neuronal differentiation;Calzari;Mol. Neurobiol.,2020
4. BMAL1 associates with NOP58 in the nucleolus and contributes to pre-rRNA processing;Cervantes;iScience,2020
5. Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity;Coe;Nat. Genet,2019
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