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


KALKAN UÇAR S. , Canda E., ÇOKER M.

SSIEM 2016 Annual Symposium, Rome, Italy. J Inherit Metab Dis 2016; 39 ( suppl 1 ): S160., 6 - 09 September 2016

  • Publication Type: Conference Paper / Summary Text