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

Bildiriler > Özet Bildiri · 2016

Yazarlar: Sema KALKAN UÇAR, Ebru CANDA, Mahmut ÇOKER

SSIEM 2016 Annual Symposium, Rome, Italy. J Inherit Metab Dis 2016; 39 ( suppl 1 ): S160., Uluslararası, Özet Bildiri, 2016-2016