Entries of Thiel, C. on the publication server

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. Fulltext not available.