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    1. p38α Regulates Expression of DUX4 in a Model of Facioscapulohumeral Muscular Dystrophy

      by Rahl, Peter; Ronco, Lucienne; Cadavid, Diego; Robertson, Alan; Chang, Aaron N.; Maglio, Joseph; Valentine, Erin; Shen, Ning; Cacace, Angela M.; Thompson, Lorin A.; et al.

      The Journal Of Pharmacology And Experimental Therapeutics, Volume 374, Issue 3, pp. 489 - 498

      Journal Article : Full Text Online

    2. Ultrarare Muscular Dystrophy Mimics Facioscapulohumeral Muscular Dystrophy

      by Gardner, Bret J. and Cardon, Meeta

      Pediatric Neurology, Volume 161, pp. 99 - 100

      Journal Article : Full Text Online

    3. DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent (...)

      by Harper, Scott Q.; Wallace, Lindsay M.; Mei, Wenyan; Ladner, Katherine J.; Belayew, Alexandra; Yang, Jing; Coppee, Frederique; Guttridge, Denis and Garwick, Sara E.

      Annals Of Neurology, Volume 69, Issue 3, pp. 540 - 552

      Journal Article : Full Text Online

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    1. Muscular Dystrophy : Methods and Protocols

      edited by Katherine M.D. Bushby, Louise V.B. Anderson.

      Book : View Online

    2. Muscular Dystrophy Therapeutics : Methods and Protocols

      edited by Rika Maruyama, Toshifumi Yokota.

      Book : View Online

    3. Knuckleball : A Sit-Down Comedian Stands Up to Muscular Dystrophy

      Connell Creations (Firm).

      Book, Video : View Online

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    1. Unraveling the complex etiology of a simple Mendelian disease

      by Kristen Lee Deak.

      Archival and manuscript material

      Check Holdings for this item's availability University Archives, Medical Center Library

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