Search Results - Shimakura, Yae

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  1. 1
    Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans

    Failure to find evidence for association between voltage-gated sodium channel gene SCN2A variants and febrile seizures in humans by Nakayama, Junko, Yamamoto, Nao, Hamano, Kenzo, Iwasaki, Nobuaki, Ohta, Masayasu, Nakahara, Satoko, Horigome, Yumi, Nakahara, Chieko, Noguchi, Emiko, Shiono, Junko, Shimakura, Yae, Yamakawa-Kobayashi, Kimiko, Matsui, Akira, Arinami, Tadao

    Published in Neuroscience letters
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  2. 2
    Frequent Occurrence of Hypoalphalipoproteinemia Due to Mutant Apolipoprotein A-I Gene in the Population: A Population-Based Survey

    Frequent Occurrence of Hypoalphalipoproteinemia Due to Mutant Apolipoprotein A-I Gene in the Population: A Population-Based Survey by Yamakawa-Kobayashi, Kimiko, Yanagi, Hisako, Fukayama, Hiromi, Hirano, Chiaki, Shimakura, Yae, Yamamoto, Nao, Arinami, Tadao, Tsuchiya, Shigeru, Hamaguchi, Hideo

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  3. 3
    A novel complex mutation in the LDL receptor gene probably caused by the simultaneous occurrence of deletion and insertion in the same region

    A novel complex mutation in the LDL receptor gene probably caused by the simultaneous occurrence of deletion and insertion in the same region by Yamakawa-Kobayashi, K, Kobayashi, T, Yanagi, H, Shimakura, Y, Satoh, J, Hamaguchi, H

    Published in Human genetics
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  4. 4
    Family studies of the LDL receptor gene of relatively severe hereditary hypercholesterolemia associated with Achilles tendon xanthomas

    Family studies of the LDL receptor gene of relatively severe hereditary hypercholesterolemia associated with Achilles tendon xanthomas by YAMAKAWA, K, YANAGI, H, ARAKAWA, K, HAMAGUCHI, H, SAKU, K, SASAKI, J, OKAFUJI, T, SHIMAKURA, Y, KAWAI, K, TSUCHIYA, S, TAKADA, K, NAITO, S

    Published in Human genetics
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