Works by Jinhong Wie


Results: 16
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    GABBR2 mutations determine phenotype in rett syndrome and epileptic encephalopathy.

    Published in:
    2017
    By:
    • Yoo, Yongjin;
    • Jung, Jane;
    • Lee, Yoo‐Na;
    • Lee, Youngha;
    • Cho, Hyosuk;
    • Na, Eunjung;
    • Hong, JeaYeok;
    • Kim, Eunjin;
    • Lee, Jin Sook;
    • Lee, Je Sang;
    • Hong, Chansik;
    • Park, Sang‐Yoon;
    • Wie, Jinhong;
    • Miller, Kathryn;
    • Shur, Natasha;
    • Clow, Cheryl;
    • Ebel, Roseànne S.;
    • DeBrosse, Suzanne D.;
    • Henderson, Lindsay B.;
    • Willaert, Rebecca
    Publication type:
    journal article
    12

    Intellectual disability-associated UNC80 mutations reveal inter-subunit interaction and dendritic function of the NALCN channel complex.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-17105-8
    By:
    • Wie, Jinhong;
    • Bharthur, Apoorva;
    • Wolfgang, Morgan;
    • Narayanan, Vinodh;
    • Ramsey, Keri;
    • C4RCD Research Group;
    • Belnap, Newell;
    • Claasen, Ana;
    • Courtright, Amanda;
    • de Both, Matt;
    • Huentelman, Matthew;
    • Rangasamy, Sampathkumar;
    • Richholt, Ryan;
    • Schrauwen, Isabelle;
    • Siniard, Ashley L.;
    • Szelinger, Szabolics;
    • Aranda, Kimberly;
    • Zhang, Qi;
    • Zhou, Yandong;
    • Ren, Dejian
    Publication type:
    Article
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