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Schulz M, Malherbe C, Cheng B, Thomalla G, Schlemm E
They need comprehensive toxicology testing, detailed genomic risk assessments for virulence and antimicrobial resistance genes, and rigorous phase IIII clinical trials, similar to other LBPs (525)
10.1007/s10552-013-0272-3 298
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Acta 67 , 207212 (1976)
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