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Clinical Monitoring in a Patient with Friedreich Ataxia and Osteogenic Sarcoma
Friedreich ataxia is an autosomal recessive neurodegenerative disorder caused by mutations in the FXN gene that result in abnormally low levels of the mitochondrial protein frataxin. We recently used a lateral flow immunoassay to measure frataxin levels in a large cohort of controls, carriers, and p...
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| Main Authors: | , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
2012
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3674811/ https://ncbi.nlm.nih.gov/pubmed/22752483 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/0883073812448460 |
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