Congenital disorder of glycosylation with defective fucosylation 2 (FCSK gene defect): The third report in the literature with a mild phenotype
Abstract Background Congenital disorders of glycosylation (CDG) are a group of heterogeneous disorders caused by abnormal lipid or protein glycosylation. Variants in the FCSK gene have been reported to cause CDG. Defective FCSK‐induced CDG (FCSK–CDG) has only been reported previously in three unrela...
المؤلفون الرئيسيون: | , , , , , , , , , , , |
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التنسيق: | مقال |
اللغة: | English |
منشور في: |
Wiley
2023-04-01
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سلاسل: | Molecular Genetics & Genomic Medicine |
الموضوعات: | |
الوصول للمادة أونلاين: | https://doi.org/10.1002/mgg3.2117 |