D-2-hydroxyglutaric aciduria: biochemival marker or clinical disease entity?

M.S. van der Knaap; C.A.J.M. Jakobs; G.F. Hoffmann; M. Duran; A.C. Muntau; S. Schweitzer; R.I. Kelley; F. Parrot-Rouland; J. Amiel; P. De Lonlay; O. Rabier; O. Eeg-Olofsson

doi:10.1023/A:1005548005393

D-2-hydroxyglutaric aciduria: biochemival marker or clinical disease entity?

M.S. van der Knaap, C.A.J.M. Jakobs, G.F. Hoffmann, M. Duran, A.C. Muntau, S. Schweitzer, R.I. Kelley, F. Parrot-Rouland, J. Amiel, P. De Lonlay, O. Rabier, O. Eeg-Olofsson

Research output: Contribution to Journal › Article › Academic

Original language	English
Pages (from-to)	404-413
Journal	Journal of Inherited Metabolic Disease
Volume	22
DOIs	https://doi.org/10.1023/A:1005548005393
Publication status	Published - 1999
Externally published	Yes

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10.1023/A:1005548005393

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van der Knaap, M. S., Jakobs, C. A. J. M., Hoffmann, G. F., Duran, M., Muntau, A. C., Schweitzer, S., Kelley, R. I., Parrot-Rouland, F., Amiel, J., De Lonlay, P., Rabier, O., & Eeg-Olofsson, O. (1999). D-2-hydroxyglutaric aciduria: biochemival marker or clinical disease entity? Journal of Inherited Metabolic Disease, 22, 404-413. https://doi.org/10.1023/A:1005548005393

@article{015cbdf22aa6450aba8a0a136911a242,

title = "D-2-hydroxyglutaric aciduria: biochemival marker or clinical disease entity?",

author = "\{van der Knaap\}, M.S. and C.A.J.M. Jakobs and G.F. Hoffmann and M. Duran and A.C. Muntau and S. Schweitzer and R.I. Kelley and F. Parrot-Rouland and J. Amiel and \{De Lonlay\}, P. and O. Rabier and O. Eeg-Olofsson",

year = "1999",

doi = "10.1023/A:1005548005393",

language = "English",

volume = "22",

pages = "404--413",

journal = "Journal of Inherited Metabolic Disease",