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Browsing by Author "Fujihara, Noriko"

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Issue DateTitleAuthor(s)
Aug-2010 A C-terminal amino acid substitution in the γ-chain caused by a novel heterozygous frameshift mutation (Fibrinogen Matsumoto VII) results in hypofibrinogenaemiaFujihara, Noriko; Haneishi, Ayumi; Yamauchi, Kazuyoshi; Terasawa, Fumiko; Ito, Toshiro; Ishida, Fumihiro; Okumura, Nobuo; 山内, 一由
Oct-2011 Factor H gene variants in Japanese: Its relation to atypical hemolytic uremic syndromeMukai, Saki; Hidaka, Yoshihiko; Hirota-Kawadobora, Masako; Matsuda, Kazuyuki; Fujihara, Noriko; Takezawa, Yuka; Kubota, Seiko; Koike, Kenichi; Honda, Takayuki; Yamauchi, Kazuyoshi; 山内, 一由
Sep-2010 In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A > G causing abnormal RNA splicingTerasawa, Fumiko; Kamijyo, Yuka; Fujihara, Noriko; Yamauchi, Kazuyoshi; Kumagai, Toshiko; Honda, Takayuki; Shigematsu, Satoshi; Okumura, Nobuo; 山内, 一由
Showing results 1 to 3 of 3

 

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