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RFT1-CDG: deafness as a novel feature of congenital disorders of glycosylation.
Jaeken, J; Vleugels, W; Régal, L; Corchia, C; Goemans, N; Haeuptle, M A; Foulquier, F; Hennet, T; Matthijs, G; Dionisi-Vici, C.
Affiliation
  • Jaeken J; Center for Metabolic Disease, University of Leuven, Leuven, Belgium. jaak.jaeken@uzleuven.be
J Inherit Metab Dis ; 32 Suppl 1: S335-8, 2009 Dec.
Article in En | MEDLINE | ID: mdl-19856127
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Congenital Disorders of Glycosylation / Hearing Loss, Sensorineural Type of study: Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: J Inherit Metab Dis Year: 2009 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Membrane Glycoproteins / Congenital Disorders of Glycosylation / Hearing Loss, Sensorineural Type of study: Prognostic_studies Limits: Female / Humans / Infant / Male / Newborn Language: En Journal: J Inherit Metab Dis Year: 2009 Document type: Article