DOI: 10.1055/s-00046370

Global Medical Genetics

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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