Morisada, N., Hamada, R., Miura, K., Ye, M. J., Nozu, K., Hattori, M., & Iijima, K. (2020). Bardet–Biedl syndrome in two unrelated patients with identical compound heterozygous SCLT1 mutations. CEN Case Rep.

Morisada, Naoya, Riku Hamada, Kenichiro Miura, Ming Juan Ye, Kandai Nozu, Motoshi Hattori, and Kazumoto Iijima. "Bardet–Biedl Syndrome in Two Unrelated Patients With Identical Compound Heterozygous SCLT1 Mutations." CEN Case Rep 2020.

Morisada, Naoya, et al. "Bardet–Biedl Syndrome in Two Unrelated Patients With Identical Compound Heterozygous SCLT1 Mutations." CEN Case Rep 2020.