Results 1 - 1 of 1 for "Homocystinuria-Megaloblastic" anemia due to defect in cobalamin "metabolism," cblE complementation type
  1. Genetics Home Reference: Homocystinuria From the National Institutes of Health (National Library of Medicine)  
    ... Homocystinuria due to CBS deficiency Genetic Testing Registry: Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Genetic Testing Registry: METHYLCOBALAMIN DEFICIENCY, cblG TYPE Genetic ...
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