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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

Dwight D. Koeberl

Division of Medical Genetics

Duke University Medical Center

Durham

USA

[email]@mc.duke.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Division of Medical Genetics, Duke University Medical Center, Durham, USA. 2003 - 2012

References

  1. In search of proof-of-concept: gene therapy for glycogen storage disease type Ia. Koeberl, D.D. J. Inherit. Metab. Dis. (2012) [Pubmed]
  2. 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) [Pubmed]
  3. 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) [Pubmed]
 
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