J. Muroi
Department of Pediatrics
Kyoto University Hospital
Japan
Name/email consistency: high
- Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency. Muroi, J., Yorifuji, T., Uematsu, A., Shigematsu, Y., Onigata, K., Maruyama, H., Nobutoki, T., Kitamura, A., Nakahata, T. Hum. Genet. (2000)
- Identification of a novel single base-pair polymorphism in the glutamate dehydrogenase (GLUD1) gene. Muroi, J., Uematsu, A., Yorifuji, T. J. Hum. Genet. (1999)