Electroencephalographic findings and genetic characterization of two brothers with IQSEC2 pathogenic variant
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health
Reference17 articles.
1. Next-generation sequencing in X-linked intellectual disability;Tzschach;Eur J Hum Genet,2015
2. Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability;Tran Mau-Them;Eur J Hum Genet,2014
3. Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders;Moey;Eur J Hum Genet,2016
4. The molecular and phenotypic spectrum of IQSEC2-related epilepsy;Zerem;Epilepsia,2016
5. Developmental progression of intellectual disability, autism, and epilepsy in a child with an IQSEC2 gene mutation;Zipper;Clin Case Rep,2017
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Preliminary Study on Clinical Characteristics and Pathogenesis of IQSEC2 Mutations Patients;Pharmacogenomics and Personalized Medicine;2024-05
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