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

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Published in Seizure on September 08, 2011

Authors

Alexa K Craig1, Marcio Sotero de Menezes, Russell P Saneto

Author Affiliations

1: Division of Pediatric Neurology, Seattle Children's Hospital/University of Washington, 4800 Sand Point Way NE, Seattle, WA 98105, United States.

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