Author:
Heymans H. S. A.,Oorthuys J. W. E.,Nelck G.,Wanders R. J. A.,Dingemans K. P.,Schutgens R. B. H.
Subject
Genetics (clinical),Genetics
Reference8 articles.
1. Heymans, H. S. A. Cerebro-hepato-renal (Zellweger) syndrome. Clinical and biochemical consequences of peroxisomal dysfunction.Thesis, University of Amsterdam, 1984
2. Heymans, H. S. A., Schutgens, R. B. H., Tan, R., van den Bosch, H. and Borst, P. Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).Nature (London) 306 (1983) 69–70
3. Kretzner, F. L., Hittner, H. M. and Mehta, R. Ocular manifestations of Conradi and Zellweger syndromes.Metab. Pediatr. Ophthalmol. 5 (1981) 1–11
4. Poulos, A. and Whiting, M. Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?Clin. Genet. 26 (1984) 579–586
5. Schutgens, R. B. H., Romeyn, G. J., Wanders, R. J. A., van den Bosch, H., Schrakamp, G. and Heymans, H. S. A. Deficiency of acylCoA:dihydroxyacetonephosphate acyltransferase in fibroblasts from patients with Zellweger (cerebro-hepato-renal) syndrome.Biochem. Biophys. Res. Commun. 120 (1984) 179–184
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