ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy-Reference-Cited by-同舟云学术

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ARHGAP4 variants are associated with X-linked early-onset temporal lobe epilepsy

Published:2024-07-26 Issue: Volume: Page:
ISSN:1708-8569
Container-title:World Journal of Pediatrics
language:en
Short-container-title:World J Pediatr

Author:

Hu Yuan-Yuan,Song Wang,Liu Zhi-Gang,Ye Xing-Guang,Zhang Hong-Wei,Li Xin,Luo Jun-Xia,Wang Peng-Yu,Wang Jie,Lin Xiao-Fei,Zhu Hong-Li,Liao Wei-Ping,Li Bin,Chen Xu-Qin

Funder

National Natural Science Foundation of China

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s12519-024-00830-1.pdf

Reference19 articles.

1. Foletta VC, Brown FD, Young WS 3rd. Cloning of rat ARHGAP4/C1, a RhoGAP family member expressed in the nervous system that colocalizes with the Golgi complex and microtubules. Brain Res Mol Brain Res. 2002;107:65–79.

2. Vadodaria KC, Jessberger S. Maturation and integration of adult born hippocampal neurons: signal convergence onto small Rho GTPases. Front Synaptic Neurosci. 2013;5:4.

3. Liu F, Guo H, Ou M, Hou X, Sun G, Gong W, et al. ARHGAP4 mutated in a Chinese intellectually challenged family. Gene. 2016;578:205–9.

4. Huang L, Poke G, Gecz J, Gibson K. A novel contiguous gene deletion of AVPR2 and ARHGAP4 genes in male dizygotic twins with nephrogenic diabetes insipidus and intellectual disability. Am J Med Genet A. 2012;158A:2511–8.

5. Demura M, Takeda Y, Yoneda T, Furukawa K, Usukura M, Itoh Y, et al. Two novel types of contiguous gene deletion of the AVPR2 and ARHGAP4 genes in unrelated Japanese kindreds with nephrogenic diabetes insipidus. Hum Mutat. 2002;19:23–9.

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