Reducing body myopathy update

Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. Brain 2009 132: 452-464
FHL1遺伝子変異によるreducing body myopathyの臨床的、組織学的特徴

Novel FHL1 mutations in fatal and benign reducing body myopathy. Neurology 2009 72: 375-376.
Reducing body myopathyの新たなFHL1遺伝子変異

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