Disorders of mitochondrial β-oxidation: Prenatal and early postnatal diagnosis and their relevance to Reye's syndrome and sudden infant death
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01799297
Reference44 articles.
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2. Allison, F., Barnes, I. C. S. and Bennett, M. J. The oxidation of octanoic acid by amniotic fluid cells; The effect of cell type and passage number.Prenat. Diagn. 8 (1988b) 397–398
3. Amendt, B. A., Greene, C., Sweetman, L., Cloherty, J., Shih, V., Moon, A., Teel, L. and Rhead, W. J. Short-chain acyl-CoA dehydrogenase deficiency. Clinical and biochemical studies in two patients.J. Clin. Invest. 79 (1987) 1303–1309
4. Anonymous. Sudden infant death and inherited disorders of fat oxidation.Lancet 2 (1986) 1073–1075
5. Bennett, M. J., Curnock, D. A., Engel, P. C., Shaw, L., Gray, R. G. F., Hull, D., Patrick, A. D. and Pollitt, R. J. Glutaric aciduria type II: Biochemical investigation and treatment of a child diagnosed prenatally.J. Inher. Metab. Dis. 7 (1984) 57–61
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