Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation.

Şeker-Yılmaz B., BULUT F. D., KILAVUZ S., KOR D., ARIKAN Ç., AĞIN M., ...More

14th MEMG meeting, 8 - 10 February 2018

  • Publication Type: Conference Paper / Summary Text
  • Çukurova University Affiliated: Yes