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Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II

Bibliographic reference Foulquier, F ; Vasile, E ; Schollen, E. ; Callewaert, N ; Raemaekers, T ; et. al. Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II. In: National Academy of Sciences. Proceedings, Vol. 103, no. 10, p. 3764-3769 (2006)
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