Cargando…
Expanding the phenotypic spectrum of KCNK4: From syndromic neurodevelopmental disorder to rolandic epilepsy
The KCNK4 gene, predominantly distributed in neurons, plays an essential role in controlling the resting membrane potential and regulating cellular excitability. Previously, only two variants were identified to be associated with human disease, facial dysmorphism, hypertrichosis, epilepsy, intellect...
Autores principales: | Yan, Hong-Jun, He, Yun-yan, Jin, Liang, Guo, Qiang, Zhou, Jing-Hua, Luo, Sheng |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851069/ https://www.ncbi.nlm.nih.gov/pubmed/36683851 http://dx.doi.org/10.3389/fnmol.2022.1081097 |
Ejemplares similares
-
Expanding the Phenotypic and Genotypic Spectrum of ARFGEF1-Related Neurodevelopmental Disorder
por: Xu, Lu, et al.
Publicado: (2022) -
Expansion of the mutation spectrum and phenotype of USP7-related neurodevelopmental disorder
por: Zheng, Hong, et al.
Publicado: (2022) -
Antiepileptic Drug of Levetiracetam Decreases Centrotemporal Spike-Associated Activation in Rolandic Epilepsy
por: Zhang, Qirui, et al.
Publicado: (2018) -
An updated catalog of CTCF variants associated with neurodevelopmental disorder phenotypes
por: Price, Emma, et al.
Publicado: (2023) -
Computational Evidence for a Competitive Thalamocortical Model of Spikes and Spindle Activity in Rolandic Epilepsy
por: Li, Qiang, et al.
Publicado: (2021)