Dolichol phosphate mannose synthase (DPM1) mutations define congenital disorder of glycosylation Ie (CDG-Ie)

Congenital disorders of glycosylation (CDGs) are metabolic deficiencies in glycoprotein biosynthesis that usually cause severe mental and psychomotor retardation. Different forms of CDGs can be recognized by altered isoelectric focusing (IEF) patterns of serum transferrin (Tf). Two patients with the...

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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Kim, Soohyun, Westphal, Vibeke, Srikrishna, Geetha, Mehta, Darshini P., Peterson, Sandra, Filiano, James, Karnes, Pamela S., Patterson, Marc C., Freeze, Hudson H.
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 2000
Assuntos:	Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC377427/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10642597/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI7302
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