Familial apolipoprotein C-II deficiency (Q106757): Difference between revisions
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Revision as of 13:45, 17 August 2026
This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_877401371 |
||
| English | Familial apolipoprotein C-II deficiency |
This is a deficiency in a protein that in humans is encoded by the APOC2 gene. The protein encoded by this gene is secreted in plasma where it is a component of very low density lipoproteins and chylomicrons. |
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CID11:ID_877401371
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dki-india-ID_877401371
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Concluído
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