Adelaide Research & Scholarship
Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/32925
| Citations | ||
| Scopus | Web of Science® | Altmetric |
|---|---|---|
|
?
|
?
|
|
| Type: | Journal article |
| Title: | Ornithine carbamoyltransferase deficiency presenting with chorea in a female |
| Author: | Wiltshire, E. Poplawski, N. Harbord, M. Harrison, R. Fletcher, J. |
| Citation: | Journal of Inherited Metabolic Disease, 2000; 23(8):843-844 |
| Publisher: | Kluwer Academic Publ |
| Issue Date: | 2000 |
| ISSN: | 0141-8955 1573-2665 |
| Statement of Responsibility: | E. J. Wiltshire, N. K. Poplawski, M. G. Harbord, R. J. Harrison and J. M. Fletcher |
| Keywords: | Humans Ornithine Carbamoyltransferase Deficiency Disease Chorea Orotic Acid Uracil Alanine Glutamine Infant Female |
| DOI: | 10.1023/A:1026768904395 |
| Published version: | http://dx.doi.org/10.1023/a:1026768904395 |
| Appears in Collections: | Aurora harvest Paediatrics publications |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.