SLC15A2
From Wikipedia, the free encyclopedia
This is an old revision of this page, as edited by 130.225.176.53 (talk) at 12:17, 9 May 2012 (→Further reading). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Template:PBB Solute carrier family 15 (H+/peptide transporter), member 2, also known as SLC15A2, is a human gene.[1]
See also
References
Further reading
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
see also solute carrier disorders |
This membrane protein–related article is a stub. You can help Wikipedia by expanding it. |
Retrieved from "https://en.wikipedia.org/w/index.php?title=SLC15A2&oldid=491581165"
Hidden category: