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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease

Background and aims: Recent data suggest identification of causal genetic variants for inflammatory bowel disease in the DLG5 gene and in the organic cation transporter (OCTN) cluster, both situated in previously described linkage regions. Patients and methods: The polymorphisms in DLG5 (113 G→A, 41...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Török, H-P, Glas, J, Tonenchi, L, Lohse, P, Müller-Myhsok, B, Limbersky, O, Neugebauer, C, Schnitzler, F, Seiderer, J, Tillack, C, Brand, S, Brünnler, G, Jagiello, P, Epplen, J T, Griga, T, Klein, W, Schiemann, U, Folwaczny, M, Ochsenkühn, T, Folwaczny, C
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Copyright 2005 by Gut 2005
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1774699/
https://ncbi.nlm.nih.gov/pubmed/15955786
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/gut.2005.066340
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