FOXG1 variant presenting as unexplained irritability and peculiar crying spells
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology,General Medicine
Reference6 articles.
1. Genotype-phenotype implications from three representative clinical FOXG1 variants associated with FOXG1 syndrome;Bai;Seizure,2021
2. The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis;Kortüm;J Med Genet,2011
3. FOXG1-Related Syndrome: from Clinical to Molecular Genetics and Pathogenic Mechanisms;Wong;Int J Mol Sci,2019
4. Delineating FOXG1 syndrome: from congenital microcephaly to hyperkinetic encephalopathy;Vegas;Neurol. Genet.,2018
5. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant;Bahi-Buisson;Neurogenetics,2010
Cited by 1 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. Conditional Deletion of Foxg1 Delayed Myelination during Early Postnatal Brain Development;International Journal of Molecular Sciences;2023-09-10
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