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MCB.22.20.6971-6978.2002
MCB.22.20.6971-6978.2002
http://dx.doi.org/10.1128/MCB.22.20.6971-6978.2002
Homologous recombination resolution defect in werner syndrome.
P356
Q34150355-0C279AEA-D544-486A-9865-FDF200A1848F
P356
MCB.22.20.6971-6978.2002
http://dx.doi.org/10.1128/MCB.22.20.6971-6978.2002