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  • Molecular assay reagents intended to identify mutations in the cytochrome P450 family 11 subfamily B member 1 (CYP11B1) gene, located at chromosome 8q21, which encodes the mitochondrial protein cytochrome P450 11B1. Genetic variants at this locus have been associated with familial hyperaldosteronism type 1 and deficiency of steroid 11-beta-monooxygenase.
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