Found: 2

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  • SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome.

    Published in:
    Journal of Human Genetics, 2011, v. 56, n. 12, p. 846, doi. 10.1038/jhg.2011.115
    By:
    • Hashimoto, Natsuko;
    • Kagitani-Shimono, Kuriko;
    • Sakai, Norio;
    • Otomo, Takanobu;
    • Tominaga, Koji;
    • Nabatame, Shin;
    • Mogami, Yukiko;
    • Takahashi, Yukitoshi;
    • Imai, Katsumi;
    • Yanagihara, Keiko;
    • Okinaga, Takeshi;
    • Nagai, Toshisaburo;
    • Taniike, Masako;
    • Ozono, Keiichi
    Publication type:
    Article

  • A case of cerebral hypomyelination with spondylo-epi-metaphyseal dysplasia.

    Published in:
    American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 1, p. 203, doi. 10.1002/ajmg.a.35686
    By:
    • Kimura‐Ohba, Shihoko;
    • Kagitani‐Shimono, Kuriko;
    • Hashimoto, Natsuko;
    • Nabatame, Shin;
    • Okinaga, Takeshi;
    • Murakami, Akira;
    • Miyake, Noriko;
    • Matsumoto, Naomichi;
    • Osaka, Hitoshi;
    • Hojo, Keiko;
    • Tomita, Reiko;
    • Taniike, Masako;
    • Ozono, Keiichi
    Publication type:
    Article