Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M) (Q45314786)
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An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619072)
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Defective SLC35A2 causes congenital disorder of glycosylation 2M (CDG2M) |
An instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619072) |
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