Blanchet, E., Annicotte, J., Pradelli, L. A., Hugon, G., Matecki, S., Mornet, D., . . . Fajas, L. (2012). E2F transcription factor-1 deficiency reduces pathophysiology in the mouse model of Duchenne muscular dystrophy through increased muscle oxidative metabolism. Oxford University Press.

Blanchet, Emilie, Jean-Sébastien Annicotte, Ludivine A. Pradelli, Gérald Hugon, Stéfan Matecki, Dominique Mornet, François Rivier, i Lluis Fajas. E2F Transcription Factor-1 Deficiency Reduces Pathophysiology in the Mouse Model of Duchenne Muscular Dystrophy Through Increased Muscle Oxidative Metabolism. Oxford University Press, 2012.

Blanchet, Emilie, et al. E2F Transcription Factor-1 Deficiency Reduces Pathophysiology in the Mouse Model of Duchenne Muscular Dystrophy Through Increased Muscle Oxidative Metabolism. Oxford University Press, 2012.