Canlyniadau Chwilio - 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 gan Janve, Vaishali S., Hernandez, Ciria C., Verdier, Kelienne M., Hu, Ningning, Macdonald, Robert L.

    Cyhoeddwyd 2016
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  2. 2
    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 gan Huang, Xuan, Zhou, Chengwen, Tian, Mengnan, Kang, Jing-Qiong, Shen, Wangzhen, Verdier, Kelienne, Pimenta, Aurea, Macdonald, Robert L

    Cyhoeddwyd 2017
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  3. 3
    Beyond Epilepsy and Autism: Disruption of GABRB3 Causes Ocular Hypopigmentation

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

    Cyhoeddwyd 2016
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