SLC22A5
Encyclopedia
SLC22A5 is a membrane transport protein associated with primary carnitine deficiency
.
Primary carnitine deficiency
Systemic primary carnitine deficiency , also called deficiency of plasma-membrane carnitine transporter, carnitine transporter deficiency or carnitine uptake defect , is an autosomal recessive metabolic disorder that prevents the body from using fats for energy, particularly during periods without...
.