Author:
Naseer Muhammad Imran,Abdulkareem Angham Abdulrhman,Rasool Mahmood,Shirah Bader,Algahtani Hussein,Muthaffar Osama Y.,Pushparaj Peter Natesan
Subject
General Agricultural and Biological Sciences
Reference37 articles.
1. STXBP1 encephalopathies: Clinical spectrum, disease mechanisms, and therapeutic strategies;Abramov;J. Neurochem.,2021
2. Molecular modelling and Dynamics Study of NSSNP in STXBP1 gene in early infantile epileptic encephalopathy disease;Al Mehdi;Biomed. Res. Int.,2019
3. The adult motor phenotype of Dravet syndrome is associated with mutation of the STXBP1 gene and responds well to cannabidiol treatment;Álvarez Bravo;Seizure,2018
4. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005–2009;Berg;Epilepsia,2010
5. Novel 9q34.11 gene deletions encompassing combinations of four Mendelian disease genes: STXBP1, SPTAN1, ENG, and TOR1A;Campbell;Genet. Med.: Off. J. Am. College Med. Genet.,2012