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The low nucleotide identity between SFB 16S rRNA gene sequences of human origin, and particularly within the regions targeted by popular SFB primer sets (for example, F799/R1008), has important implications for the detection of SFB using PCR-based methods (Supplementary Fig

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Mol Cell Endocrinol 410: 1118, 2015 [DOI] [PubMed] [Google Scholar] 32.Li X, Rezaei R, Li P, and Wu G

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