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  • Molecular assay reagents intended to identify deletions in the Berardinelli-Seip congenital lipodystrophy 2 (BSCL2) gene, located in 11q13, which encodes for seipin, an amino acid protein that is an integral membrane protein of the endoplasmic reticulum. Inherited deletions are associated with Berardinelli-Seip congenital lipodystrophy type 2.
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