Peroxisomal Enzyme Deficiency in the Conradi–Hunerman Form of Chondrodysplasia Punctata
- 18 June 1987
- journal article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 316 (25) , 1608
- https://doi.org/10.1056/nejm198706183162517
Abstract
Correspondence from The New England Journal of Medicine — Peroxisomal Enzyme Deficiency in the Conradi–Hunerman Form of Chondrodysplasia PunctataKeywords
This publication has 5 references indexed in Scilit:
- Peroxisomal disordersThe Journal of Pediatrics, 1986
- Deficiency of Enzymes Catalyzing the Biosynthesis of Glycerol-Ether Lipids in Zellweger SyndromeNew England Journal of Medicine, 1984
- The Cerebrohepatorenal (Zellweger) SyndromeNew England Journal of Medicine, 1984
- Heterogeneity of Chondrodysplasia punctataHuman Genetics, 1971
- Conradi's diseaseThe Journal of Pediatrics, 1968