Clinical and molecular features of congenital disorder of glycosylation in patients with type 1 sialotransferrin pattern and diverse ethnic origins
Gregory M. Enns(Lucile Packard Children's Hospital), Louanne Hudgins(Lucile Packard Children's Hospital), Gert Matthijs(VIB-KU Leuven Center for Cancer Biology), Sarina K. Behera, Charles A. Cowan(Group Health Cooperative), Robert D. Steiner(University of Wisconsin–Madison), Marjorie F. McCracken(Group Health Cooperative), Jaak Jaeken(KU Leuven), Vibeke Westphal(Sanford Burnham Prebys Medical Discovery Institute), John F. O’Brien(Mayo Clinic), Kathleen A. Leppig(Group Health Cooperative), Neil R.M. Buist(Case Western Reserve University), Hudson H. Freeze(Discovery Institute)
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