Abstract
Medium chain acyl-coenzyme A dehydrogenase deficiency (MCADD) was the first metabolic disorder found to be associated with sudden infant death syndrome. This review covers recent advances in the biochemical and molecular understanding of MCADD.
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CITATION STYLE
APA
Rice, G., Brazelton, T., Maginot, K., Srinivasan, S., Hollman, G., & Wolff, J. A. (2007). Medium Chain Acyl–Coenzyme A Dehydrogenase Deficiency in a Neonate. New England Journal of Medicine, 357(17), 1781–1781. https://doi.org/10.1056/nejmc071277
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