检索结果 - Verdier, Kelienne

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  1. 1
    EPILEPTIC ENCEPHALOPATHY DE NOVO GABRB MUTATIONS IMPAIR GABA(A) RECEPTOR FUNCTION

    EPILEPTIC ENCEPHALOPATHY DE NOVO GABRB MUTATIONS IMPAIR GABA(A) RECEPTOR FUNCTION 由 Janve, Vaishali S., Hernandez, Ciria C., Verdier, Kelienne M., Hu, Ningning, Macdonald, Robert L.

    出版 2016
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    OVEREXPRESSING WILD-TYPE γ2 SUBUNITS RESCUED THE SEIZURE PHENOTYPE IN GABRG2(+/Q390X) DRAVET SYNDROME MICE

    OVEREXPRESSING WILD-TYPE γ2 SUBUNITS RESCUED THE SEIZURE PHENOTYPE IN GABRG2(+/Q390X) DRAVET SYNDROME MICE 由 Huang, Xuan, Zhou, Chengwen, Tian, Mengnan, Kang, Jing-Qiong, Shen, Wangzhen, Verdier, Kelienne, Pimenta, Aurea, Macdonald, Robert L

    出版 2017
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    Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation

    Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation 由 Delahanty, Ryan J., Zhang, Yanfeng, Bichell, Terry Jo, Shen, Wangzhen, Verdier, Kelienne, Macdonald, Robert L., Xu, Lili, Boyd, Kelli, Williams, Janice, Kang, Jing-Qiong

    出版 2016
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