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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)
The real question is not whether you can afford Fella
Journal of Physiology (Paris), 1993, 87(5):313-327
The effectiveness of these new drugs will determine whether this pharmaceutical revolution meets its full promise
When people ask if the compounded version is as good as the branded version, they are usually asking about three things: effectiveness, safety, and consistency
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