Correspondence to: “Heterozygous mutation in the X chromosomal NDUFA1 gene in a girl with complex I deficiency” and “A novel NDUFA1 mutation leads to progressive mitochondrial complex I- specific neurodegenerative disease”
Xu, Jack Junchi, Østergaard, ElsebetVolume:
13
Language:
english
Journal:
Molecular Genetics and Metabolism Reports
DOI:
10.1016/j.ymgmr.2017.07.008
Date:
December, 2017
File:
PDF, 102 KB
english, 2017