Immune-escape mutations and stop-codons in HBsAg develop in a large proportion of patients with chronic HBV infection exposed to anti-HBV drugs in Europe.
- DOI
- 10.1186/s12879-018-3161-2
- Published
- 2018 Jun 1
- Container
- BMC infectious diseases
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1186/s12879-018-3161-2,
title = {Immune-escape mutations and stop-codons in HBsAg develop in a large proportion of patients with chronic HBV infection exposed to anti-HBV drugs in Europe.},
author = {Colagrossi L and Hermans LE and Salpini R and Di Carlo D and Pas SD and Alvarez M and Ben-Ari Z and Boland G and Bruzzone B and Coppola N and Seguin-Devaux C and Dyda T and Garcia F and Kaiser R and Köse S and Krarup H and Lazarevic I and Lunar MM and Maylin S and Micheli V and Mor O and Paraschiv S and Paraskevis D and Poljak M and Puchhammer-Stöckl E and Simon F and Stanojevic M and Stene-Johansen K and Tihic N and Trimoulet P and Verheyen J and Vince A and Lepej SZ and Weis N and Yalcinkaya T and Boucher CAB and Wensing AMJ and Perno CF and Svicher V and HEPVIR working group of the European Society for translational antiviral research (ESAR)},
year = {2018},
journal = {BMC infectious diseases},
doi = {10.1186/s12879-018-3161-2},
url = {https://doi.org/10.1186/s12879-018-3161-2}
}RIS
TY - JOUR TI - Immune-escape mutations and stop-codons in HBsAg develop in a large proportion of patients with chronic HBV infection exposed to anti-HBV drugs in Europe. AU - Colagrossi L AU - Hermans LE AU - Salpini R AU - Di Carlo D AU - Pas SD AU - Alvarez M AU - Ben-Ari Z AU - Boland G AU - Bruzzone B AU - Coppola N AU - Seguin-Devaux C AU - Dyda T AU - Garcia F AU - Kaiser R AU - Köse S AU - Krarup H AU - Lazarevic I AU - Lunar MM AU - Maylin S AU - Micheli V AU - Mor O AU - Paraschiv S AU - Paraskevis D AU - Poljak M AU - Puchhammer-Stöckl E AU - Simon F AU - Stanojevic M AU - Stene-Johansen K AU - Tihic N AU - Trimoulet P AU - Verheyen J AU - Vince A AU - Lepej SZ AU - Weis N AU - Yalcinkaya T AU - Boucher CAB AU - Wensing AMJ AU - Perno CF AU - Svicher V AU - HEPVIR working group of the European Society for translational antiviral research (ESAR) PY - 2018 JO - BMC infectious diseases DO - 10.1186/s12879-018-3161-2 UR - https://doi.org/10.1186/s12879-018-3161-2 ER -
APA
L, C., LE, H., R, S., D, D. C., SD, P., M, A., Z, B., G, B., B, B., N, C., C, S., T, D., F, G., R, K., S, K., H, K., I, L., MM, L., S, M., V, M., O, M., S, P., D, P., M, P., E, P., F, S., M, S., K, S., N, T., P, T., J, V., A, V., SZ, L., N, W., T, Y., CAB, B., AMJ, W., CF, P., V, S., & (ESAR), H. W. G. O. T. E. S. F. T. A. R. (2018). Immune-escape mutations and stop-codons in HBsAg develop in a large proportion of patients with chronic HBV infection exposed to anti-HBV drugs in Europe.. BMC infectious diseases. https://doi.org/10.1186/s12879-018-3161-2
Source records
- pubmed · retrieved 2026-09-25T17:49:21.671Z