Peroxisome Biogenesis Disorders: Identification of a New Complementation Group Distinct from Peroxisome-Deficient CHO Mutants and Not Complemented by Human PEX 13
- 1 February 1998
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 243 (2) , 368-371
- https://doi.org/10.1006/bbrc.1997.8067
Abstract
No abstract availableKeywords
Funding Information
- Ono Medical Research Foundation
- National Center of Neurology and Psychiatry
- Ministry of Education, Culture, Sports, Science and Technology
- Ministry of Health, Labour and Welfare
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