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  • Molecular assay reagents intended to identify mutations in the nuclear receptor subfamily 0, group B, member 1 (NR0B1) gene, located at chromosome Xp21.3-p21.2, which encodes for the protein DAX1 that is involved in the development and function of several hormone-producing (endocrine) tissues in the body. This genetic mutation causes congenital adrenal hypoplasia, X-linked adrenal hypoplasia congenital, and Swyer syndrome.
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