Short-chainacyl-CoA dehydrogenase deficiency: two siblings with two distinct phenotypes

Şeker-Yılmaz B., KILAVUZ S., KOR D., BULUT F. D., YILDIZDAŞ R. D., TOLUNAY İ., ...More

Annual Symposium of the Society for the Study of Inborn Errors of Metabolism, Rotterdam, The Netherlands, 3 - 06 September 2019

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