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Motor neuropathy in porphobilinogen deaminase–deficient mice imitates the peripheral neuropathy of human acute porphyria

Acute porphyrias are inherited disorders caused by partial deficiency of specific heme biosynthesis enzymes. Clinically, porphyrias are manifested by a neuropsychiatric syndrome that includes peripheral neuropathy. Although much is known about the porphyrias’ enzyme defects and their biochemical con...

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Bibliografische gegevens
Gepubliceerd in:J Clin Invest
Hoofdauteurs: Lindberg, Raija L.P., Martini, Rudolf, Baumgartner, Matthias, Erne, Beat, Borg, Jacques, Zielasek, Jürgen, Ricker, Kenneth, Steck, Andreas, Toyka, Klaus V., Meyer, Urs A.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Clinical Investigation 1999
Onderwerpen:
Online toegang:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC408280/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10207164/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI5986
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