학술논문
Homozygous missense mutation in UQCRC2 associated with severe encephalomyopathy, mitochondrial complex III assembly defect and activation of mitochondrial protein quality control
Document Type
Article
Author
Source
In: Biochimica et Biophysica Acta - Molecular Basis of Disease . (Biochimica et Biophysica Acta - Molecular Basis of Disease, 1 August 2021, 1867(8))
Subject
Language
English
ISSN
1879260X
09254439
09254439