Vasoactive intestinal peptide-expressing interneurons are impaired in a mouse model of Dravet syndrome.


Journal

eLife
ISSN: 2050-084X
Titre abrégé: Elife
Pays: England
ID NLM: 101579614

Informations de publication

Date de publication:
08 07 2019
Historique:
received: 14 03 2019
accepted: 07 07 2019
pubmed: 10 7 2019
medline: 3 3 2020
entrez: 9 7 2019
Statut: epublish

Résumé

Dravet Syndrome (DS) is a severe neurodevelopmental disorder caused by pathogenic loss of function variants in the gene

Identifiants

pubmed: 31282864
doi: 10.7554/eLife.46846
pii: 46846
pmc: PMC6629374
doi:
pii:

Substances chimiques

NAV1.1 Voltage-Gated Sodium Channel 0
Scn1a protein, mouse 0
Vasoactive Intestinal Peptide 37221-79-7

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NINDS NIH HHS
ID : F31 NS111803
Pays : United States
Organisme : NINDS NIH HHS
ID : K08 NS097633
Pays : United States
Organisme : NINDS NIH HHS
ID : R01 NS110869
Pays : United States
Organisme : Burroughs Wellcome Fund
ID : Career Award for Medical Scientists
Pays : International

Informations de copyright

© 2019, Goff and Goldberg.

Déclaration de conflit d'intérêts

KG, EG No competing interests declared

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Auteurs

Kevin M Goff (KM)

Department of Neuroscience, The University of Pennsylvania Perelman School of Medicine, Philadelphia, United States.
The Medical Scientist Training Program, The University of Pennsylvania Perelman School of Medicine, Philadelphia, United States.

Ethan M Goldberg (EM)

Department of Neuroscience, The University of Pennsylvania Perelman School of Medicine, Philadelphia, United States.
Division of Neurology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, United States.
Department of Neurology, The University of Pennsylvania Perelman School of Medicine, Philadelphia, United States.

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