| Literature DB >> 2887776 |
R W Watts, R Y Calne, K Rolles, C J Danpure, S H Morgan, M A Mansell, R Williams, P Purkiss.
Abstract
A patient with primary hyperoxaluria type 1 (hepatic peroxisomal alanine:glyoxylate aminotransferase [EC 2.6.1.44] deficiency) was successfully treated by combined hepatic and renal transplantation. The metabolic lesion was corrected by replacement of the deficient hepatic enzyme activity.Entities:
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Year: 1987 PMID: 2887776 DOI: 10.1016/s0140-6736(87)91791-0
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321