Author:
Brul S.,Wiemer E. A. C.,Strijland A.,Heymans H. S. A.,Schutgens R. B. H.,Van Den Bosch H.,Schram A. W.,Wanders R. J. A.,Westerveld A.,Tager J. M.
Reference33 articles.
1. Goldfischer, S., Moore, C.L., Johnson, A.B., Spiro, A.J., Valsamis, M.P., Wisniewski, H.K., Ritch, R.H., Norton, W.T., Rapin, I. and Gartner, L.M. (1973) Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome, Science 183, 62–64.
2. Borst, P. (1983) Animal peroxisomes (microbodies), lipid biosynthesis and the Zellweger syndrome, Trends Biochem. Sci. 8, 269–272.
3. Pedersen, J.I., and Gustafsson, J. (1980) Conversion of 3a, 7a, 12a-trihydroxy-5β-cholestanoic acid into cholic acid by rat liver peroxisomes, FEBS Lett. 121, 345-348.
4. Goldfischer, S., and Reddy, J.K. (1984) Peroxisomes (microbodies) in cell pathology, Int. Rev. Exp. Pathol. 26, 45-84.
5. Kelley, R.I., Dutta, N.S., Dabyns, W.B., Hajra, A.K., Moser, A.B., Noetzel, M.J., Zackai, E.H., and Moser, H.W. (1986) Neonatal Adrenoleukodystrophy: New cases, biochemical studies and differentiation from Zellweger and related peroxisomal polydystrophy syndromes, Am. J. Med. Genet. 23, 869-901.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献