Tomonori Kobayashi

Association between a polymorphism of ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) gene and sporadic Parkinson's disease.

S. Kubo, Kubo, Zhang, 2000, Parkinsonism & related disorders.

Clinical and genetic studies of families with the tau N279K mutation (FTDP-17)

B. Ghetti, K. Arima, R. Uitti, 2002, Neurology.

Structural dimorphism in the mitochondrial targeting sequence in the human manganese superoxide dismutase gene. A predictive evidence for conformational change to influence mitochondrial transport and a study of allelic association in Parkinson's disease.

Y. Mizuno, H. Matsumine, Y. Nakagawa-Hattori, 1996, Biochemical and biophysical research communications.

PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations

N. Hattori, H. Yoshino, R. Rosales, 2004, Neurology.