Defective Peroxisome Membrane Synthesis Due To Mutations in Human PEX3 Causes Zellweger Syndrome, Complementation Group G
- 1 October 2000
- journal article
- case report
- Published by Elsevier in American Journal of Human Genetics
- Vol. 67 (4) , 967-975
- https://doi.org/10.1086/303071
Abstract
No abstract availableKeywords
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