Mannose Phosphate Isomerase Deficiency-Congenital Disorder of Glycosylation (MPI-CDG) Type 1b: Familial Case of Thrombophilia and Liver Disorder April 3, 2025 by ccinfoadmin Clin Chem. 2025 Apr 3;71(4):523-525. doi: 10.1093/clinchem/hvaf009. NO ABSTRACT PMID:40178550 | DOI:10.1093/clinchem/hvaf009
