Abstract
Researchers from the University of Antwerp, Belgium, and numerous international collaborators report a comprehensive overview of the phenotypic and genetic spectrum of Syntaxin-binding protein 1 (STXBP1) encephalopathy.
DOI: https://doi.org/10.15844/pedneurbriefs-33-6 | Journal eISSN: 2166-6482
Language: English
Page range: 6 - 6
Submitted on: Feb 11, 2019
Accepted on: Dec 30, 2019
Published on: Dec 31, 2019
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2019 Brittani Wild, Stephen Lewis Nelson, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.
