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                                       Details for article 32 of 123 found articles
 
 
  Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects
 
 
Title: Dravet syndrome: Patients with co-morbid SCN1A gene mutations and mitochondrial electron transport chain defects
Author: Craig⁎, Alexa K.
de Menzes, Marcio Sotero
Saneto, Russell P.
Appeared in: Mitochondrion
Paging: Volume 11 (2011) nr. 4 pages 1 p.
Year: 2011
Contents:
Publisher: Published by Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 32 of 123 found articles
 
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