A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)

We describe a new congenital disorder of glycosylation, CDG-If. The patient has severe psychomotor retardation, seizures, failure to thrive, dry skin and scaling with erythroderma, and impaired vision. CDG-If is caused by a defect in the gene MPDU1, the human homologue of hamster Lec35, and is the f...

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Detalhes bibliográficos
Main Authors: Kranz, Christian, Denecke, Jonas, Lehrman, Mark A., Ray, Sutapa, Kienz, Petra, Kreissel, Gunilla, Sagi, Dijana, Peter-Katalinic, Jasna, Freeze, Hudson H., Schmid, Thomas, Jackowski-Dohrmann, Sabine, Harms, Erik, Marquardt, Thorsten
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2001
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC200991/
https://ncbi.nlm.nih.gov/pubmed/11733556
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