Clinicogenetic study of <i>PINK1</i> mutations in autosomal recessive early-onset parkinsonism
Y. Li(Juntendo University), Nobutaka Hattori(RIKEN Center for Brain Science), Mayumi Kitaguchi, Satoshi Kawaguchi(Sapporo Medical University), Yoshikuni Mizuno(Juntendo University), Hiroaki Miyajima(Koei Chemical (Japan)), Katsuya Sato, Hideaki Yoshino(Hospital for Tropical Diseases), Shoichi Sasaki, Hiroyuki Tomiyama(German Center for Neurodegenerative Diseases), Yasuko Hatano, Masahiko Atsumi, Tatsushi Toda(Osaka University)
Cited by 138
Related Papers
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
|Nature Genetics|2000|2k
PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy
|The Journal of Cell Biology|2010|1.9k