A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip
Article
Rind, N., Schmeiser, V., Thiel, C., Absmanner, B., Lubbehusen, J., Hocks, J., Apeshiotis, N., Wilichowski, E., Lehle, L. and Korner, C. (2010) A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip. Human Molecular Genetics 19 (8), pp. 1413-1424.Alternative links to fulltext
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Details
| Item type | Article | ||||
| Journal or Publication Title | Human Molecular Genetics | ||||
| Publisher | OXFORD UNIV PRESS | ||||
| Place of Publication | OXFORD | ||||
| Volume | 19 | ||||
| Number of Issue or Book Chapter | 8 | ||||
| Page Range | pp. 1413-1424 | ||||
| Date | 2010 | ||||
| Date of publication | 19 Dec 2024 11:38 | ||||
| Institutions | Biology, Preclinical Medicine > Institut für Pflanzenwissenschaften | ||||
| Identification Number |
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| Keywords | LINKED OLIGOSACCHARIDE BIOSYNTHESIS; SACCHAROMYCES-CEREVISIAE; N-GLYCOSYLATION; CDG-II; ALG11; RETICULUM; YEAST; GENE; | ||||
| Dewey Decimal Classification | 500 Science > 580 Botanical sciences | ||||
| Status | Published | ||||
| Refereed | Yes, this version has been refereed | ||||
| Created at the University of Regensburg | Yes | ||||
| Item ID | 66189 |
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