authors
- Marshall, Aren E
- Brady, Lauren
- Yeh, Ed
- Mears, Alan J
- Lacaria, Melanie
- Chakraborty, Pranesh
- Tarnopolsky, Mark
- Kernohan, Kristin D
Next generation sequencing reveals novel compound heterozygous deletions in NDUFAF2 in a child with mitochondrial complex I deficiency, nuclear type 10
Journal Articles
- Overview
- Research
- Identity
- Additional Document Info
- View All
Overview
status
publication date
- July 2024
has subject area
- 0604 Genetics (FoR)
- 1103 Clinical Sciences (FoR)
- Child (MeSH)
- Electron Transport Complex I (MeSH)
- Female (MeSH)
- Heterozygote (MeSH)
- High-Throughput Nucleotide Sequencing (MeSH)
- Humans (MeSH)
- Male (MeSH)
- Mitochondrial Diseases (MeSH)
- Sequence Deletion (MeSH)