Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation

✍ Scribed by Morava, E; Lefeber, D J; Urban, Z; de Meirleir, L; Meinecke, P; Gillessen Kaesbach, G; Sykut-Cegielska, J; Adamowicz, M; Salafsky, I; Ranells, J

• Book ID: 110027246
• Publisher: Nature Publishing Group
• Year: 2007
• Tongue: English
• Weight: 233 KB
• Volume: 16
• Category: Article
• ISSN: 1018-4813
• DOI: 10.1038/sj.ejhg.5201947