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Description
At a Glance There is currently no genetic cure for Systemic Primary Carnitine Deficiency (SPCD) because it is caused by a permanent mutation

In: Kramer K, Hoppe P, Packer L, eds

Functional and molecular studies in primary carnitine deficiency

J Clin Oncol

L-carnitine is believed to work by altering insulin receptors and changing the expression of specific genes that regulate sugar metabolism
