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    Postprint
    Consortium of Swiss Academic Libraries

    Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient

    Rimella-Le-Huu, A. ; Henry, H. ; Kern, I. ; Hanquinet, S. ; Roulet-Perez, E. ; Newman, C. ; Superti-Furga, A. ; Bonafé, L. ; Ballhausen, D.

    In: Journal of Inherited Metabolic Disease, 2008, vol. 31, p. 381-386

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