Primary biochemical defect in copper metabolism in mice with a recessive X-linked mutation analogous to Menkes' disease in man
- 1 January 1979
- journal article
- research article
- Published by Elsevier in Journal of Inorganic Biochemistry
- Vol. 10 (1) , 19-27
- https://doi.org/10.1016/s0162-0134(00)81002-8
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- Catecholamine biosynthesis and the activity of a number of copper-dependent enzymes in the copper deficient mottled mouse mutantsComparative Biochemistry and Physiology Part C: Comparative Pharmacology, 1977
- Primary defect in copper transport underlies mottled mutants in the mouseNature, 1974
- MENKES'S KINKY HAIR SYNDROMEPediatrics, 1972