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0.5 mL monomethylamine reagent (MeOH/H 2 O/n-butanol/CH 3 NH 2 solution

Produced in a facility that handles milk, soy, eggs, fish, celery, cereals containing gluten, and products thereof

Expiry Date: March 31, 2027 Remaining Period: 11 months

If a patient does not tolerate the 2.4 mg once-weekly maintenance dose, the dose may be reduced to 1.7 mg once weekly

Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter

This motif is present in the Na + -driven hOCTN1 and mOCTN3, but notably absent in OCTs and OATs, suggesting a possible OCTN-specific role of this motif