Mitochondrial glutamate carrier 1 deficiency (Q94615)
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This is a deficiency predominantly expressed in the plasma membrane, allowing it to remove glutamate from the extracellular space. It has also been localised in the inner mitochondrial membrane as part of the malate-aspartate shuttle.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_358582965 |
||
| English | Mitochondrial glutamate carrier 1 deficiency |
This is a deficiency predominantly expressed in the plasma membrane, allowing it to remove glutamate from the extracellular space. It has also been localised in the inner mitochondrial membrane as part of the malate-aspartate shuttle. |
