Schessl, J., Taratuto, A. L., Sewry, C., Battini, R., Chin, S. S., Maiti, B., . . . Bönnemann, C. G. (2009). Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. Oxford University Press.
Citación estilo ChicagoSchessl, Joachim, et al. Clinical, Histological and Genetic Characterization of Reducing Body Myopathy Caused By Mutations in FHL1. Oxford University Press, 2009.
Cita MLASchessl, Joachim, et al. Clinical, Histological and Genetic Characterization of Reducing Body Myopathy Caused By Mutations in FHL1. Oxford University Press, 2009.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.