Peroxisomal abnormalities in rhizomelic chondrodysplasia punctata
- 1 June 1986
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 9 (S2) , 329-331
- https://doi.org/10.1007/bf01799743
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
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- Infantile Refsum's disease (phytanic acid storage disease): a variant of Zellweger's syndrome?Clinical Genetics, 1984
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- Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndromeBiochemical and Biophysical Research Communications, 1984
- Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome)Nature, 1983
- Heterogeneity of Chondrodysplasia punctataHuman Genetics, 1971