Molecular genetic analysis of a novel <i>Parkin</i> gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in the <i>Parkin</i> gene in affected individualsNobutaka Hattori, Yoshikuni Mizuno, Tohru Kitada et al.|Annals of Neurology|1998Cited by 294
Point Mutations (Thr240Arg and Ala311Stop) in theParkinGeneNobutaka Hattori, Yoshikuni Mizuno, Mei Wang et al.|Biochemical and Biophysical Research Communications|1998Cited by 180
Mitochondrial dysfunction in parkinson's diseaseYoshikuni Mizuno, Tomoyoshi Kondo, Hiroyo Yoshino et al.|Annals of Neurology|1998Cited by 164
Analyses of the MAPT, PGRN, and C9orf72 mutations in Japanese patients with FTLD, PSP, and CBSKotaro Ogaki, Nobutaka Hattori, Yuanzhe Li et al.|Parkinsonism & Related Disorders|2012Cited by 93
Polymorphism in theparkin gene in sporadic Parkinson's diseaseMei Wang, Yoshikuni Mizuno, Nobutaka Hattori et al.|Annals of Neurology|1999Cited by 87