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Results 1 - 4 of 4 for Congenital disorders of glycosylation type II
  1. ... and dysfunction in the first COG4-deficient CDG type II patient. Hum Mol Genet. ... for a human glycosylation disorder caused by mutation of the COG4 gene. Proc ...
  2. Immune System and Disorders (National Library of Medicine)  
    What is the immune system? Your immune system is a complex network of cells, tissues, and organs. Together they help the body fight infections and other ...
  3. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
  4. ... dystrophy Walker-Warburg syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 1; MDDGA1 MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH ...