Neurotransmitters and Sodium Channelopathies; Possible Link?
Abstract
Investigators from the University of British Columbia, Great Ormond Street Hospital for Children, and the National Hospital reported their findings on neurotransmitter deficiencies in two patients with mutations in voltage-gated sodium genes (SCN2A and SCN8A) discovered by whole exome sequencing.
DOI: https://doi.org/10.15844/pedneurbriefs-31-3-1 | Journal eISSN: 2166-6482
Language: English
Page range: 7 - 7
Submitted on: Mar 3, 2017
Accepted on: Mar 23, 2017
Published on: Nov 10, 2017
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
Keywords:
© 2017 Michael F. Hammer, Alejandra D.C. Encinas, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.