DOI:
10.1055/s-00046370
Global Medical Genetics
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References
Foulquier F, Vasile E, Schollen E. et al.
Conserved oligomeric Golgi complex subunit 1 deficiency reveals a previously uncharacterized congenital disorder of glycosylation type II.
Proc Natl Acad Sci U S A 2006;
103 (10) 3764-3769
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