Abnormal glutathione conjugation in patients with tyrosinaemia type I

Autor: Gerard J. Mulder, T. M. T. Mulders, Douwe D. Breimer, D. J. W. Bergman, Gerrit Smit, Marinus Duran, Jan A.M. Smeitink, B. T. Poll-The

Publikováno v: Journal of inherited metabolic disease, 20(4), 473-485. Springer Netherlands
Journal of Inherited Metabolic Disease, 20, 473-485
Journal of Inherited Metabolic Disease, 20, pp. 473-485

Previous studies have suggested that tyrosinaemia type I may be associated with reduced glutathione availability due to conjugation of tyrosinaemia-associated reactive intermediates with glutathione. In the present study, the glutathione/ glutathione

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c35d70a82d76c0809b9732bb42487705
https://doi.org/10.1023/a:1005385009831