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Protein-coding gene in the species Homo sapiens
Aldehyde dehydrogenase 16 family, member A1 also known as ALDH16A1 is an aldehyde dehydrogenase gene.
Clinical significance [ edit ]
Mutations in the SPG21 (ACP33/maspardin) gene are associated with the mast syndrome, a type of spastic paraplegia . The protein encoded by the SPG21 gene has been shown to interact with the ALDH16A1 enzyme.[ 5]
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