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  • Molecular assay reagents intended to identify mutations in the AFG3 like matrix AAA peptidase subunit 2 (AFG3L2) gene, located at chromosome 18p11, which encodes the protein AFG3-like protein 2. Genetic variants at this locus have been associated with autosomal recessive spastic ataxia 5 and spinocerebellar ataxia 28.
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