Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. (Q39819541)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation. |
scientific article |
Statements
Defining the phenotype in an autosomal recessive cutis laxa syndrome with a combined congenital defect of glycosylation (English)
Morava E
Lefeber DJ
de Meirleir L
Meinecke P
Gillessen Kaesbach G
Adamowicz M
Salafsky I
Ranells J
Lemyre E
van Reeuwijk J
Brunner HG
31 October 2007
1 reference
1 reference