A severe human metabolic disease caused by deficiency of...

Human Molecular Genetics 2010 / 04 Vol. 19; Iss. 8

A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip

Rind, N., Schmeiser, V., Thiel, C., Absmanner, B., Lubbehusen, J., Hocks, J., Apeshiotis, N., Wilichowski, E., Lehle, L., Korner, C.
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Volume:
19
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/ddq016
Date:
April, 2010
File:
PDF, 426 KB
english, 2010
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