super mic b complex with l carnitine Kirkland Signature Super B-Complex with
Description
USA 102 , 83098314 (2005)
Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)
doi: 10.1007/s12035-009-8056-1
Adv Pediatr 42:209242 Badve MS, Bhuta S, McGill J (2015) Rare presentation of a treatable disorder: glutaric aciduria type 1
