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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Manylion Llyfryddiaeth

Cyhoeddwyd yn:	J Clin Invest
Prif Awduron:	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
Fformat:	Artigo
Iaith:	Inglês
Cyhoeddwyd:	American Society for Clinical Investigation 1988
Pynciau:	Research Article
Mynediad Ar-lein:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC442615/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2454948/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113510
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