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rhIGF-1 Therapy for Growth Failure and IGF-1 Deficiency in Congenital Disorder of Glycosylation Ia (PMM2 Deficiency)

Background. Congenital disorders of glycosylation (CDG) are a group of rare disorders in which glycosylation required for proper protein-protein interactions and protein stability is disrupted, manifesting clinically with multiple system involvement and growth failure. The insulin-like growth factor...

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Detalles Bibliográficos
Autores principales:	Miller, Bradley S., Duffy, Meghann M., Addo, O. Yaw, Sarafoglou, Kyriakie
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	SAGE Publications 2013
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4586814/ https://www.ncbi.nlm.nih.gov/pubmed/26425584 http://dx.doi.org/10.1177/2324709613503316

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