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Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation
Morava, E, Lefeber, D J, Urban, Z, de Meirleir, L, Meinecke, P, Gillessen Kaesbach, G, Sykut-Cegielska, J, Adamowicz, M, Salafsky, I, Ranells, JVolume:
16
Year:
2007
Language:
english
Pages:
8
DOI:
10.1038/sj.ejhg.5201947
File:
PDF, 233 KB
english, 2007