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Severe hyperammonemia in a newborn infant with methylmalonyl-CoA mutase deficiency.
Authors:S Packman  M J Mahoney  K Tanaka  Y E Hsia
Affiliation:1. Department of Pediatrics, Division of Genetics University of California, San Francisco, Calif., USA;2. Department of Human Genetics, Yale University School of Medicine, New Haven, Conn., USA;3. Department of Pediatrics, Yale University School of Medicine, New Haven, Conn., USA;4. Department of Genetics, University of Hawaii at Manoa, Honolulu, Hawaii, USA;5. Department of Pediatrics, University of Hawaii at Manoa, Honolulu, Hawaii, USA
Abstract:
Keywords:Reprint address: Division of Genetics   Department of Pediatrics   University of California   San Francisco   San Francisco   CA 94143.
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