1989Pediatric ResearchOpen access

Genetic and Phenotypic Heterogeneity in Disorders of Peroxisome Biogenesis—A Complementation Study Involving Cell Lines from 19 Patients

Adelbert A. Roscher, Sigrid Hoefler, Gerald Höefler, Eduard Paschke, Fritz Paltauf, Ann B. Moser, Hugo W. Moser

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Key concepts: Complementation, Zellweger syndrome, Phenotype, Peroxisomal disorder, Biology, Genotype, Genetics, Genetic heterogeneity

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