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Aicardi-Goutières Syndrome Is Caused by IFIH1 Mutations
Authors:Hirotsugu Oda  Kenji Nakagawa  Junya Abe  Tomonari Awaya  Masahide Funabiki  Atsushi Hijikata  Ryuta Nishikomori  Makoto Funatsuka  Yusei Ohshima  Yuji Sugawara  Takahiro Yasumi  Hiroki Kato  Tsuyoshi Shirai  Osamu Ohara  Takashi Fujita  Toshio Heike
Institution:1 Department of Pediatrics, Kyoto University Graduate School of Medicine, Kyoto 6068507, Japan;2 Laboratory for Integrative Genomics, RIKEN Center for Integrative Medical Sciences, Yokohama 2300045, Japan;3 Department of Pediatrics, Kitano Hospital, Tazuke Kofukai Medical Research Institute, Osaka 5308480, Japan;4 Laboratory of Molecular Genetics, Institute for Virus Research, Kyoto University, Kyoto 6068507, Japan;5 Department of Bioscience, Nagahama Institute of Bio-Science and Technology, Nagahama 5260829, Japan;6 Department of Pediatrics, Tokyo Women’s Medical University, Tokyo 1628666, Japan;7 Department of Pediatrics, Faculty of Medical Sciences, University of Fukui, Fukui 9108507, Japan;8 Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo 1138510, Japan;9 Precursory Research for Embryonic Science and Technology (PRESTO), Science and Technology Agency (JST), Kawaguchi 3320012, Japan;10 Department of Human Genome Research, Kazusa DNA Research Institute, Kisarazu 2920818, Japan
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