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Mutations in mitochondrial complex I assembly factor NDUFAF3 cause Leigh syndrome
Fabian Baertling1, Laura Sánchez-Caballero2, Sharita Timal2
1Department of Pediatrics, Radboud Centre for Mitochondrial Medicine, Radboud University Medical Centre, Geert Grooteplein Zuid 10, 6525 GA Nijmegen, The Netherlands; Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital Duesseldorf, Heinrich Heine University, Moorenstr. 5, 40225 Düsseldorf, Germany.
NDUFAF3 deficiency causes severe mitochondrial disease. This study identifies Leigh syndrome as a new clinical feature, linking NDUFAF3 to complex I assembly and expanding understanding of mitochondrial disorders.
Area of Science:
- Mitochondrial biology
- Genetics
- Biochemistry
Background:
- NDUFAF3 is crucial for mitochondrial respiratory chain complex I assembly.
- Mutations in NDUFAF3 are known to cause severe multisystem mitochondrial disease.
- Leigh syndrome is a severe neurological disorder typically affecting infants and young children.
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