Newborn screening by tandem mass spectrometry for glutaric aciduria type 1: a cost-effectiveness analysis

BACKGROUND: Glutaric aciduria type I (GA-I) is a rare metabolic disorder caused by inherited deficiency of glutaryl-CoA dehydrogenase. Despite high prognostic relevance of early diagnosis and start of metabolic treatment as well as an additional cost saving potential later in life, only a limited nu...

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Bibliografiset tiedot
Päätekijät: Pfeil, Johannes, Listl, Stefan, Hoffmann, Georg F, Kölker, Stefan, Lindner, Martin, Burgard, Peter
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2013
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4015693/
https://ncbi.nlm.nih.gov/pubmed/24135440
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-8-167
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