FCDGC: Expansion of Molecular and Phenotypic Features of ALG8-CDG Suggests Improvements for Clinical Management
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15 de ago. de 2022 ·
1m 51s
New research from the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC). This summary is based on a paper published in the Journal of Inherited Metabolic Disease on June 18,...
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New research from the Frontiers in Congenital Disorders of Glycosylation Consortium (FCDGC). This summary is based on a paper published in the Journal of Inherited Metabolic Disease on June 18, 2022, titled "ALG8-CDG: Molecular and phenotypic expansion suggests clinical management guidelines."
Read the paper here: https://onlinelibrary.wiley.com/doi/10.1002/jimd.12527
Learn more about FCDGC: https://www.rarediseasesnetwork.org/fcdgc
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Read the paper here: https://onlinelibrary.wiley.com/doi/10.1002/jimd.12527
Learn more about FCDGC: https://www.rarediseasesnetwork.org/fcdgc
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