Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Genetics(clinical),Genetics
Reference19 articles.
1. Goodman, S. I., Markey, S. P., Moe, P. G., Miles, B. S., Teng, C. C. (1975) Glutaric aciduria; a 'new' disorder of amino acid metabolism. Biochem. Med. 12: 12–21
2. Haworth JC, Booth FA, Chudley AE, et al (1991) Phenotypic variation in glutaric aciduria type 1: report of fourteen cases in five Canadian Indian kindreds. J Pediatr 118:52–58
3. Goodman SI, Kratz LE, DiGiulio KA, Biery BJ, Goodman KE, Isaya G, Frerman FE (1995) Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli. Hum. Molec. Genet. 4:1493–1498
4. Brismar J, Ozand PT (1995) CT and MR of the brain in glutaric academia type 1: a review of 59 published cases and a report of 5 new patients. AJNR 16:675–683
5. Kölker S, Koeller DM, Okun JG, Hoffmann GF (2004) Pathomechanisms of neurodegeneration in glutaryl-CoA dehydrogenase deficiency. Ann Neurol 55:7–12
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