Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

D.E. Neilson, M.D. Adams, C.M.D. Orr, D.K. Schelling, R.M. Eiben, D.S. Kerr, J. Anderson, A.G. Bassuk, A.M. Bye, A.M. Childs, A. Clarke, Y.J. Crow, M. Di Rocco, C. Dohna-Schwake, G. Dueckers, A.E. Fasano, A.D. Gika, D. Gionnis, M.P. Gorman, P.J. Grattan-SmithA. Hackenberg, A. Kuster, M.G. Lentschig, E. Lopez-Laso, E.J. Marco, S. Mastroyianni, J. Perrier, T. Schmitt-Mechelke, S. Servidei, A. Skardoutsou, P. Uldall, M.S. van der Knaap, K.C. Goglin, D.L. Tefft, C. Aubin, P. de Jager, D. Hafler, M.L. Warman

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)44-51
JournalAmerican journal of human genetics
Issue number1
Publication statusPublished - 2009

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