Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus
Yanick J. Crow(University of Leeds), Bruce E. Hayward(University of Leeds), Rekha Parmar(University of Leeds), Peter Robins(Cancer Research UK), Andrea Leitch(Western General Hospital), Manir Ali(University of Leeds), Deborah N. Black(Montreal Neurological Institute and Hospital), Hans van Bokhoven(Radboud University Nijmegen), Han G. Brunner(Radboud University Nijmegen), Ben C.J. Hamel(Radboud University Nijmegen), Peter Corry(St. Luke's Hospital), Frances M. Cowan(Hammersmith Hospital), Suzanna G.M. Frints(Maastricht University Medical Centre), Joerg Klepper(Essen University Hospital), John H. Livingston(Leeds General Infirmary), Sally Ann Lynch(Children's Health Ireland at Crumlin), R. Massey(Hull Royal Infirmary), Jean François Meritet(Université Paris Cité), Jacques L. Michaud(Centre Hospitalier Universitaire Sainte-Justine), G Ponsot(Université Paris Cité), Thomas Voït(Essen University Hospital), Pierre Lebon(Université Paris Cité), David T. Bonthron(University of Leeds), Andrew P. Jackson(Western General Hospital), Deborah E. Barnes(Cancer Research UK), Tomas Lindahl(Cancer Research UK)
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