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...

Descripción completa

Detalles Bibliográficos
Autores principales: Park, Hyo Jin, Jung, Eun Suk, Kong, Kyoung Ae, Park, Eun-Mi, Cheon, Jae Hee, Choi, Ji Ha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786794/
https://www.ncbi.nlm.nih.gov/pubmed/26965072
http://dx.doi.org/10.1038/srep22887

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4786794/
https://www.ncbi.nlm.nih.gov/pubmed/26965072
http://dx.doi.org/10.1038/srep22887

Ejemplares similares