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G.P.115 Recurrent myoglobinuria and deranged acyl-carnitines due to mutation of the COII gene of mtDNA
Vissing, C.R., Duno, M., Wibrand, F., Vissing, J.Volume:
22
Language:
english
Journal:
Neuromuscular Disorders
DOI:
10.1016/j.nmd.2012.06.287
Date:
October, 2012
File:
PDF, 47 KB
english, 2012