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Rabenstein M, Weis J, Abicht A, et al. Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II: schwierige Diagnose, einfache Therapie. [Multiple acyl-CoA dehydrogenase deficiency/glutaric aciduria type 2: difficult diagnosis, easy to treat]. Nervenarzt. 2020;91(4):349-352doi: 10.1007/s00115-020-00886-0.
Rabenstein, M., Weis, J., Abicht, A., Fink, G. R., Lehmann, H. C., & Wunderlich, G. (2020). Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II: schwierige Diagnose, einfache Therapie. [Multiple acyl-CoA dehydrogenase deficiency/glutaric aciduria type 2: difficult diagnosis, easy to treat]. Der Nervenarzt, 91(4), 349-352. https://doi.org/10.1007/s00115-020-00886-0
Rabenstein, M, et al. "Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II: schwierige Diagnose, einfache Therapie." [Multiple acyl-CoA dehydrogenase deficiency/glutaric aciduria type 2: difficult diagnosis, easy to treat]. Der Nervenarzt vol. 91,4 (2020): 349-352. doi: https://doi.org/10.1007/s00115-020-00886-0
Rabenstein M, Weis J, Abicht A, Fink GR, Lehmann HC, Wunderlich G. Multipler Acyl-CoA-Dehydrogenase-Mangel/Glutarazidurie Typ II: schwierige Diagnose, einfache Therapie. [Multiple acyl-CoA dehydrogenase deficiency/glutaric aciduria type 2: difficult diagnosis, easy to treat]. Nervenarzt. 2020 Apr;91(4):349-352. doi: 10.1007/s00115-020-00886-0. German. PMID: 32076759.
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