Erythrocyte Lactate Transporter Defect, also known as metabolic myopathy due to lactate transporter defect,is related to monocarboxylate transporter 1 deficiency and hyperinsulinemic hypoglycemia, familial, 7,and has symptoms including elevated serum creatine phosphokinase, exercise-induced muscle cramps and exercise-induced muscle stiffness. An important gene associated with Erythrocyte Lactate Transporter Defect is SLC16A1 (Solute Carrier Family 16 Member 1)

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Pathways Associated With Trait

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