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Volume 16, Number 7—July 2010

Research

High Diversity and Ancient Common Ancestry of Lymphocytic Choriomeningitis Virus

Cesar G. Albariño1Comments to Author , Gustavo Palacios1, Marina L. Khristova, Bobbie R. Erickson, Serena A. Carroll, James A. Comer, Jeffrey Hui, Thomas Briese, Kirsten St. George, Thomas G. Ksiazek2, W. Ian Lipkin, and Stuart T. Nichol
Author affiliations: Centers for Disease Control and Prevention, Atlanta, Georgia, USA (C.G. Albariño, M.L. Khristova, B.R. Erickson, S.A. Carroll, J.A. Comer, T.G. Ksiazek, S.T. Nichol); Columbia University, New York, New York, USA (G. Palacios, J. Hui, T. Briese, W.I. Lipkin); New York State Department of Health, Albany, New York, USA (K. St. George)

Main Article

Appendix Figure 4

Schematic of lymphocytic choriomeningitis virus (LCMV) GPC open reading frame. The protein motifs previously identified in the Armstrong strain, such as the 2 hydrophobic domains in the signal peptide, the myristoylation site in G2, and most of the potential glycosylation sites found in other arenaviruses, are well conserved (34).

Appendix Figure 4. Schematic of lymphocytic choriomeningitis virus (LCMV) GPC open reading frame. The protein motifs previously identified in the Armstrong strain, such as the 2 hydrophobic domains in the signal peptide, the myristoylation site in G2, and most of the potential glycosylation sites found in other arenaviruses, are well conserved (34).

Main Article

1These authors contributed equally to this article.

2Current affiliation: University of Texas Medical Branch, Galveston, Texas, USA.

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