ArticleIntractable & rare diseases research2025
A novel ETFDH mutation identified in a patient with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.
Yaotong Ou et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
ArticleIntractable & rare diseases research2025
Yaotong Ou et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.