Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

Generalized peroxisome-deficient disorders including cerebro-hepato-renal Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease are autosomal recessive diseases, where catalase-containing particles (peroxisomes) are morphologically absent. We previously isolated two Chinese...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:J Clin Invest
Päätekijät: Shimozawa, N, Tsukamoto, T, Suzuki, Y, Orii, T, Fujiki, Y
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: American Society for Clinical Investigation 1992
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443247/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1430210/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116063
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