A rare missense variant abrogates the signaling activity of tetherin/BST-2 without affecting its effect on virus release
Daniel Sauter(Institute of Medical Microbiology and Hygiene), Frank Kirchhoff(Universität Ulm), Christian Kubisch(University of Bonn), Dominik Hotter(Boehringer Ingelheim (Germany)), Fabian Giehler(Helmholtz Zentrum München), Susanne Engelhart(Universität Ulm), Arnd Kieser(Helmholtz Zentrum München)
Cited by 31
Related Papers
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
|Nature Genetics|2006|1.2k
A Potassium Channel Mutation in Neonatal Human Epilepsy
|Science|1998|1.1k
Absence of Intact nef Sequences in a Long-Term Survivor with Nonprogressive HIV-1 Infection
|New England Journal of Medicine|1995|1k