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Paper Details

Protease-dependent defects in N-cadherin processing drive PMM2-CDG pathogenesis.
JCI Insight
4
2021
CDG, Congenital Disorders of Glycosylation, N, N-cadherin, PMM2, PMM2-, cartilage defects, matrix metalloproteinase, matrix metalloproteinases, mutant embryos, patient, phosphomannomutase, pmm2 sa10150, pmm2sa10150, pmm2sa10150 mutant, zebrafish
Author NameAffiliation
Zhi-Jie XiaSanford Children's Health Research Center, Sanford Burnham Prebys Medical Discovery Institute
Peggi M AngelMedical University of South Carolina
Richard R DrakeMedical University of South Carolina
Hudson H FreezeSanford Children's Health Research Center, Sanford Burnham Prebys Medical Discovery Institute
Richard SteetComplex Carbohydrate Research Center, University of Georgia
Richard SteetJC Self Research Institute
Heather Flanagan-SteetComplex Carbohydrate Research Center, University of Georgia
Heather Flanagan-SteetJC Self Research Institute
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Release 1.2