Schaefer AM
No ORCID on file
· 1 paper in corpus
· active 2020
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Frequent coauthors
- Falkous G 1
- Hopton S 1
- Hardy SA 1
- Loher D 1
- Lilleker JB 1
- Ng YS 1
- Roberts ME 1
- Shaunak S 1
- Thompson K 1
- Taylor RW 1
2020
Mitochondrial complex I deficiency is associated with a diverse range of clinical phenotypes and can arise due to either mitochondrial DNA (mtDNA) or nuclear gene defects. We investigated two adult patients who exhibited non-syndromic neuro…