Mitochondrial defect and PGC-1α dysfunction in parkin-associated familial Parkinson’s disease

Authors: Pacelli C., De Rasmo D., Signorile A., Grattagliano I., di Tullio G., D’Orazio A., Nico B., Comi G.P., Ronchi D., Ferranini E., Pirolo D., Seibel P., Schubert S., Gaballo A., Villani G., Cocco T.
Years: 2011
Source Title: Biochimica et Biophysica Acta – Molecular Basis of Disease
Doi: 10.1016/j.bbadis.2010.12.022
Venue: CNR Nanotec @ Lecce