Mitochondrial aspartate glutamate carrier 1 deficiency (Q94608)

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_1277104703
English	Mitochondrial aspartate 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.