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- W2019930456 abstract "Abstract Congenital disorders of glycosylation include a group of diseases, each of them caused by different protein (mostly enzyme) impairment due to a specific gene defect. The many subtypes are classified according to clinical features, enzymology and molecular genetic analyses. Problems in diagnostics arise from the great diversity in clinical presentation, usually age-related, and different severities of individual types of these, by far underdiagnosed, diseases. Also the biochemical findings tend to vary, even within a single type. No one screening test, common for all types, is available so far. Several methods of choice may be used in the first approach; other procedures must follow for detailed typing of the defect. Possible drawbacks and pitfalls in the diagnostics from the viewpoint of our 3-year studies and practical screening experience are presented." @default.
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- W2019930456 date "2004-01-07" @default.
- W2019930456 modified "2023-09-23" @default.
- W2019930456 title "Pitfalls and drawbacks in screening of congenital disorders of glycosylation" @default.
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- W2019930456 doi "https://doi.org/10.1515/cclm.2004.101" @default.
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