Search Results - Izawa K

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    Clinical heterogeneity among a three-generation Japanese family with D18N <it>TREX1</it> mutation for Aicardi-Goutières syndrome / familial chilblain lupus by Heike T, Yasumi T, Kawai T, Awaya T, Izawa K, Nishikomori R, Abe J, Hiragi N, Hiragi T

    Published 2011
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    Diagnosis of NLRP3 somatic mosaicism in CINCA/NOMID patients using next-generation sequencing by Nakahata T, Kawai T, Yasumi T, Aksentijevich I, Goldbach-Mansky R, Saito MK, Tanikaze N, Nishikomori R, Izawa K, Heike T, Ohara O

    Published 2011
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