M. Nishizawa

Identification of binding sites for anti-aquaporin 4 antibodies in patients with neuromyelitis optica

T. Nakada, M. Tsujita, K. Sakimura, 2009, Journal of Neuroimmunology.

Crigler-Najjar syndrome type II is inherited both as a dominant and as a recessive trait.

Y. Adachi, O. Koiwai, T. Kamisako, 1996, Human molecular genetics.

Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase.

Y. Adachi, O. Koiwai, O Koiwai, 1995, Human molecular genetics.

Genome-wide association study identifies a new susceptibility locus in PLA2G4C for Multiple System Atrophy.

Sonja W. Scholz, A. Singleton, Y. Kusakabe, 2023, medRxiv.

Lack of Association of Serotonin 2A Receptor Gene in Japanese Patients with Obstructive Sleep Apnea Syndrome

M. Ota, Hiroshi Yamamoto, M. Yasuo, 2017 .