Mitochondrial defect and PGC-1α dysfunction in parkin-associated familial Parkinson's disease-Reference-Cited by-同舟云学术

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

Published:2011-08 Issue:8 Volume:1812 Page:1041-1053
ISSN:0925-4439
Container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
language:en
Short-container-title:Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Author:

Pacelli Consiglia,De Rasmo Domenico,Signorile Anna,Grattagliano Ignazio,di Tullio Giuseppe,D'Orazio Andria,Nico Beatrice,Comi Giacomo Pietro,Ronchi Dario,Ferranini Ermanno,Pirolo Domenico,Seibel Peter,Schubert Susanna,Gaballo Antonio,Villani Gaetano,Cocco Tiziana

Funder

Italian Ministry for the University (MIUR)

University of Bari

Sächsische Ministerium für Wissenschaft und Kunst (SMWK)

Publisher

Elsevier BV

Subject

Molecular Biology,Molecular Medicine

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3. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism;Kitada;Nature,1998