which cardiac drugs use organic cation transporter novel type 2 for uptake?
Would this then interfere with carnitine uptake? Does the transporter have a greater affinity for the drugs or the carnitine?
Public Comments
- http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12214846&dopt=Abstract
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