The contribution of OCTN1/2 variants within the IBD5 locus to disease susceptibility and severity in Crohn’s disease

<p style="text-align:justify;"><b>Background &amp; Aims:</b> Recent data suggest that polymorphisms in the organic cation transporter (OCTN) genes OCTN1 (SLC22A4) and OCTN2 (SLC22A5) represent disease-causing mutations within the IBD5 locus (chromosome 5q31). We inve...

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Bibliografske podrobnosti
Main Authors: Noble, C, Nimmo, E, Drummond, H, Ho, G, Tenesa, A, Smith, L, Anderson, N, Arnott, I, Satsangi, J
Format: Journal article
Jezik:English
Izdano: Elsevier 2005