A new mutation of mitochondrial DNAJC19 in a Turkish patient with 3 methylglutaconic aciduria dysmorphic feature dilated cardiomyopathy dystonia anemia male genital anomalies and deafness

Conference paper > Summary Text · 2016

Authors: Sema KALKAN UÇAR, Ebru CANDA, Mahmut ÇOKER

SSIEM 2016 Annual Symposium, Rome, Italy. J Inherit Metab Dis 2016; 39 ( suppl 1 ): S160., International, Summary Text, 2016-2016

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