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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...
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| Asıl Yazarlar: | , , , , , , , , , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Copyright 2005 by Gut
2005
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| Konular: | |
| Online Erişim: | 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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