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Article

Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids.

Journal of inherited metabolic disease - 1 Jan 1992

Mandel H, Berant M, Aizin A, Gershony R, Hemmli S, Schutgens R B, Wanders R J

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Identifiers

PMID: 1405475
DOI: 10.1007/BF02435982

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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Zellweger-like phenotype in two siblings: a defect in peroxisomal beta-oxidation with elevated very long-chain fatty acids but normal bile acids.PMID 1405475Read ↗

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Zellweger Syndrome: A Case Report.Semantic proximity Read ↗

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Zellweger syndrome and associated phenotypes.Semantic proximity Read ↗

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Zellweger spectrum disorders: clinical overview and management approach.Semantic proximity Read ↗

Diagnostic challenges and disease management in patients with a mild Zellweger spectrum disorder phenotype.Semantic proximity Read ↗

Genetic and molecular bases of peroxisome biogenesis disorders.Semantic proximity Read ↗

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