Mutations in PMM2 that cause congenital disorders of glycosylation, type Ia (CDG-Ia)
Gert Matthijs(VIB-KU Leuven Center for Cancer Biology), Bryan Winchester(Great Ormond Street Hospital), Hudson H. Freeze(Discovery Institute), Sandrine Vuillaumier‐Barrot(Université Claude Bernard Lyon 1), Faiqa Imtiaz(King Faisal Specialist Hospital & Research Centre), Søren K. Kjærgaard(Rigshospitalet), M. Schwartz(University of Copenhagen), Cecilia Bjursell, Vibeke Westphal(Sanford Burnham Prebys Medical Discovery Institute), Tommy Martinsson(University of Gothenburg), Els Schollen(KU Leuven), Nathalie Séta(Assistance Publique – Hôpitaux de Paris), Anna Erlandson
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