Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Congenital Disorders of Glycosylation and TF[original query] |
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Genetic variants of transferrin in the diagnosis of protein hypoglycosylation. Journal of inherited metabolic disease 2006 1 28 (6): 1184-8. Albahri Z, Marklová E, Vanícek H, Minxová L, Dédek P, Skálová |
Genetic variants of transferrin in cystic fibrosis. Journal of inherited metabolic disease 2008 Jun 31 (3): 457-61. Marklová E, Albahri Z, Vanícek H, Dedek P, Valis M, Kopácová M, Vávrová |
Fast screening of N-glycosylation disorders by sialotransferrin profiling with capillary zone electrophoresis. Annals of clinical biochemistry 2018 5 55 (6): 693-701. Kingma H A, van der Sluijs F H, Heiner-Fokkema M |
Congenital disorders of glycosylation: Prevalence, incidence and mutational spectrum in the Polish population. Molecular genetics and metabolism reports 2021 Jun 27 100726. Lipi?ski Patryk, Bogda?ska Anna, Tylki-Szyma?ska An |
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