Neurotransmitters and Sodium Channelopathies; Possible Link?
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
Publié dans: | Pediatric neurology briefs. - 1997. - 31(2017), 3 vom: 09. Nov., Seite 7 |
---|---|
Auteur principal: | |
Autres auteurs: | |
Format: | Article en ligne |
Langue: | English |
Publié: |
2017
|
Accès à la collection: | Pediatric neurology briefs |
Sujets: | Journal Article Comment Channelopathy Dopamine Nav1.2 Nav1.6 SCN2A SCN8A Seizures Serotonin |
Accès en ligne |
Volltext |