Viruses infecting bivalve molluscs
Aquat. Living Resour., 17 4 (2004) 397-409
Published online: 2004-10-15
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395 (2011)
https://doi.org/10.1002/9780470960967.ch14
Experimental ostreid herpesvirus 1 infection of the Pacific oyster Crassostrea gigas: Kinetics of virus DNA detection by q-PCR in seawater and in oyster samples
D. Schikorski, N. Faury, J.F. Pepin, et al.Virus Research 155 (1) 28 (2011)
https://doi.org/10.1016/j.virusres.2010.07.031