Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/32925
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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
RMID: 0001003044
DOI: 10.1023/A:1026768904395
Appears in Collections:Paediatrics publications

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