Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis.

We have used complementation analysis after somatic cell fusion to investigate the genetic relationships among various genetic diseases in humans in which there is a simultaneous impairment of several peroxisomal functions. The activity of acyl-coenzyme A:dihydroxyacetonephosphate acyltransferase, w...

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Detalhes bibliográficos
Main Authors: Brul, S, Westerveld, A, Strijland, A, Wanders, R J, Schram, A W, Heymans, H S, Schutgens, R B, van den Bosch, H, Tager, J M
Formato: Artigo
Idioma:Inglês
Publicado em: 1988
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC442615/
https://ncbi.nlm.nih.gov/pubmed/2454948
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