T., G., A., M., G., H., N., N., C., B., P., V., . . . C., G. (2017). Deep sequencing is an appropriate tool for the selection of unique Hepatitis C virus (HCV) variants after single genomic amplification.
Chicago Style CitationT., Guinoiseau, Moreau A., Hohnadel G., Ngo-Giang-Huong N., Brulard C., Vourc'H P., Goudeau A., and Gaudy-Graffin C. Deep Sequencing Is an Appropriate Tool for the Selection of Unique Hepatitis C Virus (HCV) Variants After Single Genomic Amplification. 2017.
MLA CitationT., Guinoiseau, et al. Deep Sequencing Is an Appropriate Tool for the Selection of Unique Hepatitis C Virus (HCV) Variants After Single Genomic Amplification. 2017.
Warning: These citations may not always be 100% accurate.