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- W2068836467 abstract "The peroxisomal disorders represent a genetically determined group of diseases in man in which there is an impairment in one or more peroxisomal functions. The different disorders known today are usually divided into three groups depending upon whether there is a generalized (A), multiple (B) or single (C) loss of peroxisomal functions (for review see Wanders et al 1988; Lazarow and Moser 1989). At present two distinct disorders have been recognized to belong to group B, which includes Zellweger-like syndrome and rhizomelic chondrodysplasia punctata (RCDP)" @default.
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- W2068836467 date "1992-05-01" @default.
- W2068836467 modified "2023-10-18" @default.
- W2068836467 title "Human dihydroxyacetonephosphate acyltransferase deficiency: A new peroxisomal disorder" @default.
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- W2068836467 doi "https://doi.org/10.1007/bf02435984" @default.
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