Authors:
Muroi, J
Yorifuji, T
Uematsu, A
Shigematsu, Y
Onigata, K
Maruyama, H
Nobutoki, T
Kitamura, A
Nakahata, T
Citation: J. Muroi et al., Molecular and clinical analysis of Japanese patients with 3-hydroxy-3-methylglutaryl CoA lyase (HL) deficiency, HUM GENET, 107(4), 2000, pp. 320-326
Authors:
Muroi, J
Yorifuji, T
Uematsu, A
Nakahata, T
Citation: J. Muroi et al., Cerebral infarction and pancreatitis: possible complications of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency, J INH MET D, 23(6), 2000, pp. 636-637
Citation: J. Muroi et al., Identification of a novel single base-pair polymorphism in the glutamate dehydrogenase (GLUD1) gene, J HUM GENET, 44(4), 1999, pp. 268-269
Authors:
Yorifuji, T
Muroi, J
Uematsu, A
Hiramatsu, H
Momoi, T
Citation: T. Yorifuji et al., Hyperinsulinism-hyperammonemia syndrome caused by mutant glutamate dehydrogenase accompanied by novel enzyme kinetics, HUM GENET, 104(6), 1999, pp. 476-479