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Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1
Schessl, J., Taratuto, A. L., Sewry, C., Battini, R., Chin, S. S., Maiti, B., Dubrovsky, A. L., Erro, M. G., Espada, G., Robertella, M., Saccoliti, M., Olmos, P., Bridges, L. R., Standring, P., Hu, Y.Volume:
132
Language:
english
Journal:
Brain
DOI:
10.1093/brain/awn325
Date:
June, 2008
File:
PDF, 1.09 MB
english, 2008