Complex I deficiency remains the most frequent cause of Leigh syndrome spectrum
This scientific commentary refers to 'Biallelic <i>NDUFA13</i> variants lead to a neurodevelopmental phenotype with gradual neurological impairment', by Kaiyrzhanov <i>et al</i>. (https://doi.org/10.1093/braincomms/fcae453).
Authors
- Shamima Rahman (ORCID: https://orcid.org/0000-0003-2088-730X)
Institutions
- Institute of Child Health (GR)
- University College London (GB)
Publication Details
- Journal
- Brain Communications
- Published
- 2024-12-23
- DOI
- https://doi.org/10.1093/braincomms/fcae470
- Citations
- 6
- Primary Topic
- Mitochondrial Function and Pathology
- Type
- article
- Field-Weighted Citation Impact
- 1.40
Funders
- National Institute for Health and Care Research
- Great Ormond Street Hospital Charity
- Lily Foundation
- National Institutes of Health
- NIHR Great Ormond Street Hospital Biomedical Research Centre