Login / Signup
Evaluation of burden of SCN1A pathogenicity in North Indian children with Dravet syndrome.
Sandeep Negi
Prateek Bhatia
Anupriya Kaur
Jhumki Das
Tanvi Bhatia
Ritu Aggarwal
Naveen Sankhyan
Pratibha Singhi
Jitendra Kumar Sahu
Published in:
Seizure (2024)
This work represents a genetic analysis of a Dravet syndrome cohort, revealing a 58 % burden of SCN1A variants in children with the Dravet syndrome phenotype from the North Indian population.
Keyphrases
</>
young adults
case report
risk factors
genome wide
escherichia coli