Glycosphingolipid synthesis is impaired in SLC35A2-CDG and improves with galactose supplementation
Abstract SLC35A2-CDG is an X-linked congenital disorder of glycosylation (CDG), characterized by defective UDP-galactose transport into the Golgi and endoplasmic reticulum and consequent insufficient galactosylation of glycans. Clinically, this translates into a range of predominantly neurological s...
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Main Authors: | , , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Springer
2025-06-01
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Series: | Cellular and Molecular Life Sciences |
Subjects: | |
Online Access: | https://doi.org/10.1007/s00018-025-05759-w |
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