Show 5 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Minczuk, M" or (type exact bookEditor and editor="Minczuk, M") Add to list Conference Paper C3 Two siblings with myopathy, mild mental retardation and combined OXPHOS deficiencies caused by a mutation in the gene encoding asparaginyl tRNA synthetase, NARS2 Arnaud Vanlander (UGent) , M Minczuk, Tom Sante (UGent) , Joél Smet (UGent) , Boel De Paepe (UGent) , Linda De Meirleir, Björn Menten (UGent) and Rudy Van Coster (UGent) (2014) JOURNAL OF INHERITED METABOLIC DISEASE. 37(1, suppl. 1). p.S39-S39