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  • Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.

    Published in:
    Brain: A Journal of Neurology, 2009, v. 132, n. 2, p. 452, doi. 10.1093/brain/awn325
    By:
    • Joachim Schessl;
    • Ana L. Taratuto;
    • Caroline Sewry;
    • Roberta Battini;
    • Steven S. Chin;
    • Baijayanta Maiti;
    • Alberto L. Dubrovsky;
    • Marcela G. Erro;
    • Graciela Espada;
    • Monica Robertella;
    • Maria Saccoliti;
    • Patricia Olmos;
    • Leslie R. Bridges;
    • Peter Standring;
    • Ying Hu;
    • Yaqun Zou;
    • Kathryn J. Swoboda;
    • Mena Scavina;
    • Hans-Hilmar Goebel;
    • Christina A. Mitchell
    Publication type:
    Article