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These additional causes include sporadic genetic disorders, such as spinocerebellar atrophy type 27B, caused by GAA expansion in the FGF14 gene, and cerebellar ataxia with neuropathy and vestibular areflexia syndrome (CANVAS), caused by biallelic expansions in the RFC1 gene
For dietary deficiency without neurological involvement, oral supplementation may be appropriate
Min JH, Sarlus H, Harris RA
This decline coincides with reduced healing capacity, slower tissue regeneration, and accelerated aging
They are fragile
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