bibliographic resource 493540 [br/493540]
https://w3id.org/oc/corpus/br/493540

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title
  • A frequent mild mutation in ALG6 may exacerbate the clinical severity of patients with congenital disorder of glycosylation Ia (CDG-Ia) caused by phosphomannomutase deficiency
publication date
  • 2002-01-01
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