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Transferrin D protein variants in the diagnosis of congenital disorders of glycosylation (CDG)

Congenital disorders of glycosylation are a rapidly growing group of inherited (neuro)metabolic disorders characterized by defects in glycosylation of proteins and lipids. This study discusses an analytical problem in the differentiation between hypoglycosylation and transferrin (Tf) protein variant...

詳細記述

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書誌詳細
出版年:J Clin Lab Anal
主要な著者: Marklová, Eliška, Albahri, Ziad
フォーマット: Artigo
言語:Inglês
出版事項: Wiley Subscription Services, Inc., A Wiley Company 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6648993/
https://ncbi.nlm.nih.gov/pubmed/19288450
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.20293
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