SLC22A18
Template:PBB Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.[1][2][3]
See also
References
- ^ Dao D, Frank D, Qian N, O'Keefe D, Vosatka RJ, Walsh CP, Tycko B (1998). "IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes". Hum Mol Genet. 7 (4): 597–608. PMID 9499412.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M (1998). "Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples". Proc Natl Acad Sci U S A. 95 (7): 3873–8. PMC 19930. PMID 9520460.
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ignored (help)CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: SLC22A18 solute carrier family 22 (organic cation transporter), member 18".
Further reading
This article incorporates text from the United States National Library of Medicine, which is in the public domain.