Şeker-Yılmaz, B. Et Al. 2018. Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation.. 14th MEMG meeting .

Şeker-Yılmaz, B., BULUT, F. D., KILAVUZ, S., KOR, D., ARIKAN, Ç., AĞIN, M., ... ÖNENLİ MUNGAN, H. N.(2018). Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation. . 14th MEMG meeting

Şeker-Yılmaz, Berna Et Al. "Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation.," 14th MEMG meeting, 2018

Şeker-Yılmaz, Berna Et Al. "Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation.." 14th MEMG meeting , 2018

Şeker-Yılmaz, B. Et Al. (2018) . "Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation.." 14th MEMG meeting .

@conferencepaper{conferencepaper, author={Berna Şeker-Yılmaz Et Al. }, title={Hepatocerebral Mitochondrial DNA Depletion Syndrome: A Turkish Case with a MPV17 gene mutation.}, congress name={14th MEMG meeting}, city={}, country={}, year={2018}}