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Title: | Absence of common trifunctional protein mutation in patients with Alpers disease. | Austin Authors: | Yang, Z;Youil, R;Thorburn, D;Chow, C W;Cotton, R G;Baldwin, Graham S | Affiliation: | University Department of Surgery, Austin Hospital, Victoria, Australia | Issue Date: | 1-Nov-1997 | Publication information: | Journal of Inherited Metabolic Disease; 20(6): 828-30 | Gov't Doc #: | 9427153 | URI: | https://ahro.austin.org.au/austinjspui/handle/1/13565 | Journal: | Journal of inherited metabolic disease | URL: | https://pubmed.ncbi.nlm.nih.gov/9427153 | Type: | Journal Article | Subjects: | Cells, Cultured DNA.analysis.metabolism Deoxyribonucleases, Type II Site-Specific.metabolism Diffuse Cerebral Sclerosis of Schilder.genetics Fatty Acids.metabolism Fibroblasts.metabolism Humans Mitochondrial Trifunctional Protein Multienzyme Complexes.genetics Mutation Oxidation-Reduction Palmitic Acid.metabolism |
Appears in Collections: | Journal articles |
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