Previously defined variants of uncertain significance may play an important role in epilepsy and interactions between certain variants may become pathogenic

Previously defined variants of uncertain significance may play an important role in epilepsy and interactions between certain variants may become pathogenic

Abstract Objective Epilepsy is a chronic neurological disorder related to various etiologies, and the prevalence of active epilepsy is estimated to be between 4 and 10 per 1000 individuals having a significant role in genetic mutations. Next‐Generation Sequencing (NGS) panels are utilized for geneti...

Full description

Saved in:
Bibliographic Details
Main Authors: Yara Hussein, Hila Weisblum‐Neuman, Bruria Ben Zeev, Shani Stern
Format: Article
Language:English
Published: Wiley 2024-12-01
Series:Epilepsia Open
Subjects:
epilepsy
next‐generation sequencing
RANBP2
RYR3
SCN9A
variant of uncertain significance
Online Access:https://doi.org/10.1002/epi4.13085
Tags: Add Tag
No Tags, Be the first to tag this record!

Similar Items

Similar Items