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Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations
  1. Correspondence to Dr Thierry Dupré, Laboratoire Biochimie A, INSERM, 3ème étage de la tour, 46 rue Henri Huchard, 75018 Paris, France; thierry.dupre{at}bch.aphp.fr
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Dupré T, Vuillaumier-Barrot S, Chantret I, et al
Guanosine diphosphate-mannose:GlcNAc2-PP-dolichol mannosyltransferase deficiency (congenital disorders of glycosylation type Ik): five new patients and seven novel mutations

Publication history

  • Received September 22, 2009
  • Revised January 22, 2010
  • Accepted January 27, 2010
  • First published August 2, 2010.
Online issue publication 
April 27, 2016

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