Mild Phenotype Associated with

Absence seizures SLC6A1 gene autism intellectual disability myoclonic-atonic epilepsy

Journal

Journal of pediatric neurosciences

ISSN: 1817-1745

Titre abrégé: J Pediatr Neurosci

Pays: India

ID NLM: 101273794

Informations de publication

Date de publication:

Historique:

entrez: 14 9 2019

pubmed: 14 9 2019

medline: 14 9 2019

Statut: ppublish

Résumé

The Solute Carrier Family 6 Member 1 (

Identifiants

DOI: 10.4103/jpn.JPN_2_19 PMID: 31516630 PMC: PMC6712924

pubmed: 31516630

doi: 10.4103/jpn.JPN_2_19

pii: JPN-14-100

pmc: PMC6712924

doi:

Types de publication

Case Reports

Langues

eng

Pagination

100-102

Déclaration de conflit d'intérêts

There are no conflicts of interest.

Références

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Neuropharmacology. 2013 Jun;69:45-54

pubmed: 22722026

Am J Hum Genet. 2015 May 7;96(5):808-15

pubmed: 25865495

Epilepsia. 2018 Feb;59(2):389-402

pubmed: 29315614

Front Chem. 2018 Sep 11;6:397

pubmed: 30255012