학술논문
Systemic Primary Carnitine Deficiency: A Case Report with Homozygoys SLC22A5 Gene Mutation
Document Type
Article
Author
Source
In: Klinische Padiatrie . (Klinische Padiatrie, 1 July 2022, 234(4):244-245)
Subject
Language
English
ISSN
14393824
03008630
03008630