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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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Lindberg, Raija L.P., Martini, Rudolf, Baumgartner, Matthias, Erne, Beat, Borg, Jacques, Zielasek, Jürgen, Ricker, Kenneth, Steck, Andreas, Toyka, Klaus V., Meyer, Urs A.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1999
Assuntos:	Article
Acesso em linha:	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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