Dolichol kinase deficiency
From Infogalactic: the planetary knowledge core
| Dolichol kinase deficiency | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| OMIM | 610768 |
| Patient UK | Dolichol kinase deficiency |
Dolichol kinase deficiency is a cutaneous condition caused by a mutation in the dolichol kinase gene.[1][2]
It is also known as Congenital disorder of glycosylation 1m.
See also
References
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