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”
Main Authors: | Jack Junchi Xu, Elsebet Østergaard |
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Format: | Article |
Language: | English |
Published: |
Elsevier
2017-12-01
|
Series: | Molecular Genetics and Metabolism Reports |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2214426917301064 |
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