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PGM1 deficiency is recognized as the third most common N-linked Congenital Disorders of Glycosylation (CDG) in humans. Affected individuals present with liver, musculoskeletal, endocrine, and coagulation symptoms; however, the most life-threatening complication is an early onset of dilated cardiomyo...
ORGANISM(S): Mus musculus (Mouse) 
2023-08-18 | PXD036271 | Pride
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