Complex I deficiency remains the most frequent cause of Leigh syndrome spectrum.

Brain Commun

Mitochondrial Research Group, Genetics and Genomic Medicine Department, UCL Great Ormond Street Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.

Published: December 2024

This scientific commentary refers to 'Biallelic variants lead to a neurodevelopmental phenotype with gradual neurological impairment', by Kaiyrzhanov . (https://doi.org/10.1093/braincomms/fcae453).

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11733768PMC
http://dx.doi.org/10.1093/braincomms/fcae470DOI Listing

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