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Identification of OCTN2 variants and their association with phenotypes of Crohn’s disease in a Korean population

Crohn’s disease (CD) is a chronic inflammatory bowel disease and a genetic variant in the OCTN2, g.-207G > C is significantly associated with CD susceptibility. This study was aimed to identify novel OCTN2 functional promoter variants and their roles in transcriptional regulation using various in...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Park, Hyo Jin, Jung, Eun Suk, Kong, Kyoung Ae, Park, Eun-Mi, Cheon, Jae Hee, Choi, Ji Ha
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4786794/
https://ncbi.nlm.nih.gov/pubmed/26965072
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep22887
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