Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study is a research paper published in Orphanet Journal of Rare Diseases (2021). On theSindex it has a DataRank of 0. It has been cited 21 times.
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National Institute of Neurological Disorders and Stroke
Grant: U54 NS115198
National Institutes of Health
Grant: 5U54NS115198-04
Frontiers in Congenital Disorders of Glycosylation
FWCI
1.26
Citation Percentile
0.8%
Citation Trend
Fields of Study
MeSH Terms
Keywords
Sustainable Development Goals
Additional file 2 of Clinical, molecular and glycophenotype insights in SLC39A8-CDG
Additional file 2 of Clinical, molecular and glycophenotype insights in SLC39A8-CDG
Additional file 1 of Clinical, molecular and glycophenotype insights in SLC39A8-CDG
Additional file 1 of Clinical, molecular and glycophenotype insights in SLC39A8-CDG
Additional file 1 of Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study
Additional file 1 of Spontaneous improvement of carbohydrate-deficient transferrin in PMM2-CDG without mannose observed in CDG natural history study