Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/13565
Title: Absence of common trifunctional protein mutation in patients with Alpers disease.
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
Citation: Journal of Inherited Metabolic Disease; 20(6): 828-30
Internal ID Number: 9427153
URI: http://ahro.austin.org.au/austinjspui/handle/1/13565
URL: http://www.ncbi.nlm.nih.gov/pubmed/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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