Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.
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N. Callewaert | M. Krieger | W. Annaert | G. Matthijs | E. Vasile | J. Jaeken | B. Winchester | D. Quelhas | E. Schollen | F. Foulquier | P. Mills | T. Raemaekers