Dwight D. Koeberl
Division of Medical Genetics
Duke University Medical Center
Durham
USA
Name/email consistency: high
- In search of proof-of-concept: gene therapy for glycogen storage disease type Ia. Koeberl, D.D. J. Inherit. Metab. Dis. (2012)
- Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening. Koeberl, D.D., Young, S.P., Gregersen, N.S., Vockley, J., Smith, W.E., Benjamin, D.K., An, Y., Weavil, S.D., Chaing, S.H., Bali, D., McDonald, M.T., Kishnani, P.S., Chen, Y.T., Millington, D.S. Pediatr. Res. (2003)
- Evaluation of 3-methylcrotonyl-CoA carboxylase deficiency detected by tandem mass spectrometry newborn screening. Koeberl, D.D., Millington, D.S., Smith, W.E., Weavil, S.D., Muenzer, J., McCandless, S.E., Kishnani, P.S., McDonald, M.T., Chaing, S., Boney, A., Moore, E., Frazier, D.M. J. Inherit. Metab. Dis. (2003)









