Please use this identifier to cite or link to this item:
http://hdl.handle.net/20.500.12188/11557| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Starzl, T E | en_US |
| dc.contributor.author | Demetris, A J | en_US |
| dc.contributor.author | Trucco, M | en_US |
| dc.contributor.author | Ricordi, C | en_US |
| dc.contributor.author | Ildstad, S | en_US |
| dc.contributor.author | Terasaki, P I | en_US |
| dc.contributor.author | Murase, N | en_US |
| dc.contributor.author | Kendall, R S | en_US |
| dc.contributor.author | Kocova, M | en_US |
| dc.contributor.author | Rudert, W A | en_US |
| dc.date.accessioned | 2021-03-25T11:09:32Z | - |
| dc.date.available | 2021-03-25T11:09:32Z | - |
| dc.date.issued | 1993-03-18 | - |
| dc.identifier.issn | 0028-4793 | - |
| dc.identifier.uri | http://hdl.handle.net/20.500.12188/11557 | - |
| dc.description.abstract | Liver transplantation for type IV glycogen storage disease (branching-enzyme deficiency) results in the resorption of extrahepatic deposits of amylopectin, but the mechanism of resorption is not known. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Massachusetts Medical Society | en_US |
| dc.relation.ispartof | The New England journal of medicine | en_US |
| dc.title | Chimerism after liver transplantation for type IV glycogen storage disease and type 1 Gaucher's disease | en_US |
| dc.type | Article | en_US |
| dc.identifier.doi | 10.1056/NEJM199303183281101 | - |
| dc.identifier.volume | 328 | - |
| dc.identifier.issue | 11 | - |
| item.grantfulltext | none | - |
| item.fulltext | No Fulltext | - |
| crisitem.author.dept | Faculty of Medicine | - |
| Appears in Collections: | Faculty of Medicine: Journal Articles | |
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