K.M. Gibson
Department of Molecular and Medical Genetics and Pediatrics
Oregon Health & Science University
Portland 97201
USA
Name/email consistency: high
- Gamma-hydroxybutyric aciduria: a biochemist's education from a heritable disorder of GABA metabolism. Gibson, K.M. J. Inherit. Metab. Dis. (2005)
- Focal neurometabolic alterations in mice deficient for succinate semialdehyde dehydrogenase. Gibson, K.M., Schor, D.S., Gupta, M., Guerand, W.S., Senephansiri, H., Burlingame, T.G., Bartels, H., Hogema, B.M., Bottiglieri, T., Froestl, W., Snead, O.C., Grompe, M., Jakobs, C. J. Neurochem. (2002)