Login / Signup

Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation.

Damla YildizMutlu Uysal YaziciMelahat Melek OguzEmine Gulsah TorunAbdullah SezerMustafa Kiliç
Published in: Klinische Padiatrie (2022)
Keyphrases
  • replacement therapy
  • drug induced