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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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Veröffentlicht in:J Clin Invest
Hauptverfasser: Lindberg, Raija L.P., Martini, Rudolf, Baumgartner, Matthias, Erne, Beat, Borg, Jacques, Zielasek, Jürgen, Ricker, Kenneth, Steck, Andreas, Toyka, Klaus V., Meyer, Urs A.
Format: Artigo
Sprache:Inglês
Veröffentlicht: American Society for Clinical Investigation 1999
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Article
Online-Zugang: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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