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Complementation analysis in fibroblasts from eight patients with clinically different forms of citrullinaemia
Journal of Inherited Metabolic Disease
|January 1, 1981
Abstract:
We have examined the possibility of genetic heterogeneity in citrullinaemia by measuring the incorporation of [14C]citrulline into protein in PEG-induced heterokaryons derived from paired combinations of fibroblasts from eight patients with varying forms of the disease. The results are compatible with interallelic, but not intergenic, complementation in several of these fusions.