SLC22A5
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Template:PBB SLC22A5 is a membrane transport protein associated with primary carnitine deficiency.
See also
References
Further reading
External links
- SLC22A5+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- Primary Carnitine Deficiency (OCTN2 database)
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This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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see also solute carrier disorders | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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