Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) (Q45314516)
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An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619037)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) |
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619037) |
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