Work

Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects

Year: 2011

Type: article

Study design: Case Report

Source: Seizure

DOI: 10.1016/j.seizure.2011.08.010

Authors: Alexa K. Craig, Marcio Sotero de Menezes, Russell P. Saneto

Institutions: Seattle Children's Hospital, University of Washington, Swedish Medical Center

Language: English

Topic: Epilepsy research and treatment

Subfield: Psychiatry and Mental health

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: bronze

OpenAlex ID: W2007691763

FWCI: 2.407

Cites: 30

Cited by: 34

Related to: 10