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2 min read

Last Updated: 8 August 2024

FXN Gene

The FXN gene encodes frataxin, a protein essential for mitochondrial function and iron-sulphur cluster biogenesis. Mutations in the FXN gene cause Friedreich's ataxia, a neurodegenerative disorder characterised by progressive ataxia, heart disease, and diabetes. Researchers continue to study the FXN gene to develop targeted therapies for affected individuals.

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