Mitochondrial protein translation defects (Q40166): Difference between revisions
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Trata-se de defeitos na enzima que pertence à família das hidrolases, especificamente aquelas que atuam sobre anidridos de ácido para catalisar o movimento transmembrana de substâncias. | |||
| description / en | description / en | ||
This refers to defects in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances. | |||
Revision as of 05:52, 13 August 2026
This refers to defects in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C53.23 |
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| English | Mitochondrial protein translation defects |
This refers to defects in the enzyme that belongs to the family of hydrolases, specifically those acting on acid anhydrides to catalyse transmembrane movement of substances. |
