N. Wakamatsu
Department of Genetics
Central Hospital
Aichi Human Service Center
Kasugai
Japan
Name/email consistency: high
- Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung disease. Wakamatsu, N., Yamada, Y., Yamada, K., Ono, T., Nomura, N., Taniguchi, H., Kitoh, H., Mutoh, N., Yamanaka, T., Mushiake, K., Kato, K., Sonta, S., Nagaya, M. Nat. Genet. (2001)