Associated Papers
[Identification and functional analysis of combined oxidative phosphorylation deficiency 28 gene mutation].
Shi P et al.
Zhonghua Nei Ke Za Zhi, 2022
Identification and characterization of novel compound variants in SLC25A26 associated with combined oxidative phosphorylation deficiency 28.
Ji Y et al.
Gene, 2021
Select a paper to view details