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Ornithine carbamoyltransferase deficiency: Unusual clinical findings and novel mutation |
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| Authors: | V. E. Shih A. P. Safran A. H. Ropper M. Tuchman |
| Affiliation: | (1) Neurology Service, Pediatric Service, and Amino Acid Disorder Laboratory, Massachusetts General Hospital, USA;(2) Department of Neurology, Harvard Medical School, Boston, Massachusetts, USA;(3) Neurological Service P.C., Framingham, Massachusetts, USA;(4) Neurology Department, St. Elizabeth's Medical Center, Brighton, Massachusetts, USA;(5) Biochemical Genetics and Metabolism Laboratories, University of Minnesota Hospital and Clinic, Minneapolis, Minnesota, USA |
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