Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study

Peter Witters(Universitair Ziekenhuis Leuven), Éva Morava(Institut thématique Génétique, génomique et bioinformatique), Hudson H. Freeze(Discovery Institute), Kimiyo Raymond(Mayo Clinic in Arizona), Andrew C. Edmondson(Translational Therapeutics (United States)), Christin Johnsen(University of Göttingen), Marc C. Patterson(Mayo Clinic), Miao He(First Affiliated Hospital of Gannan Medical University), Christina Lam(Seattle Children's Hospital)

Orphanet Journal of Rare Diseases

February 25, 2021

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