Cargando…
Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report
The DHRS9 gene is involved in several pathways including the synthesis of allopregnanolone from progesterone. Allopregnanolone is a positive modulator of gamma aminobutyric acid (GABA) action and plays a role in the control of neuronal excitability and seizures. Whole-exome sequencing performed on a...
Autores principales: | Calì, Francesco, Elia, Maurizio, Vinci, Mirella, Vetri, Luigi, Correnti, Edvige, Trapolino, Emanuele, Roccella, Michele, Vanadia, Francesca, Romano, Valentino |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7466289/ https://www.ncbi.nlm.nih.gov/pubmed/32752300 http://dx.doi.org/10.3390/medicina56080387 |
Ejemplares similares
-
Exome sequencing in a child with neurodevelopmental disorder and epilepsy: Variant analysis of the AHNAK2 gene
por: Vinci, Mirella, et al.
Publicado: (2022) -
STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to Developmental Epileptic Encephalopathy
por: Vinci, Mirella, et al.
Publicado: (2023) -
Epilepsy: A Multifaced Spectrum Disorder
por: Vetri, Luigi, et al.
Publicado: (2023) -
Poor School Academic Performance and Benign Epilepsy with Centro-Temporal Spikes
por: Vetri, Luigi, et al.
Publicado: (2023) -
Implementation of Sample Pooling Procedure Using a Rapid SARS-CoV-2 Diagnostic Real-Time PCR Test Performed Prior to Hospital Admission of People with Intellectual Disabilities
por: Musumeci, Antonino, et al.
Publicado: (2021)