Cassereau, J., Casasnovas Pons, C., Gueguen, N., Malinge, M. C., Guillet, V., Reynier, P., . . . Chevrollier, A. (2011). Simultaneous MFN2 and GDAP1 mutations cause major mitochondrial defects in a patient with CMT.
Citación estilo ChicagoCassereau, Julien, et al. Simultaneous MFN2 and GDAP1 Mutations Cause Major Mitochondrial Defects in a Patient With CMT. 2011.
Cita MLACassereau, Julien, et al. Simultaneous MFN2 and GDAP1 Mutations Cause Major Mitochondrial Defects in a Patient With CMT. 2011.
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