Disorders of protein O-glycosylation (Q40083): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Distúrbios congênitos envolvendo defeito da ligação O-glicosilação, que normalmente ocorre através de uma ligação alfa do Glicano ao grupo hidroxilo de um resíduo de serina ou treonina em uma proteína | |||
| description / en | description / en | ||
Congenital disorders involving defective O-linked glycosylation, which typically occurs via an alpha linkage of the glycan to the hydroxyl group of a serine or threonine residue on a protein | |||
Revision as of 05:45, 13 August 2026
Congenital disorders involving defective O-linked glycosylation, which typically occurs via an alpha linkage of the glycan to the hydroxyl group of a serine or threonine residue on a protein
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C54.1 |
||
| English | Disorders of protein O-glycosylation |
Congenital disorders involving defective O-linked glycosylation, which typically occurs via an alpha linkage of the glycan to the hydroxyl group of a serine or threonine residue on a protein |
