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  • Molecular assay reagents intended to identify deletions or duplications of the Bardet-Biedl syndrome 2 (BBS2) gene, located at chromosome 16q21, which encodes the Bardet-Biedl syndrome 2 protein. Genetic variants at this locus have been associated with retinitis pigmentosa 74 and Bardet-Biedl syndrome 2.
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