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                                       Details for article 2 of 12 found articles
 
 
  A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy
 
 
Title: A novel mitochondrial ATP6 frameshift mutation causing isolated complex V deficiency, ataxia and encephalomyopathy
Author: Jackson, Christopher B.
Hahn, Dagmar
Schröter, Barbara
Richter, Uwe
Battersby, Brendan J.
Schmitt-Mechelke, Thomas
Marttinen, Paula
Nuoffer, Jean-Marc
Schaller, André
Appeared in: European journal of medical genetics
Paging: Volume 60 (2017) nr. 6 pages 7 p.
Year: 2017
Contents:
Publisher: Elsevier Masson SAS
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 2 of 12 found articles
 
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