Immunohistochemical differentiation between chronic enteropathy associated with SLCO2A1 gene and other inflammatory bowel diseases

BACKGROUND/AIMS: We recently identified recessive mutations in the solute carrier organic anion transporter family member 2A1 gene (SLCO2A1) as causative variants of chronic enteropathy associated with SLCO2A1 (CEAS). The aim of this study was to evaluate SLCO2A1 protein expression in the intestinal...

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Dades bibliogràfiques
Publicat a:Intest Res
Autors principals: Yamaguchi, Satoko, Yanai, Shunichi, Nakamura, Shotaro, Kawasaki, Keisuke, Eizuka, Makoto, Uesugi, Noriyuki, Sugai, Tamotsu, Umeno, Junji, Esaki, Motohiro, Matsumoto, Takayuki
Format: Artigo
Idioma:Inglês
Publicat: Korean Association for the Study of Intestinal Diseases 2018
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Original Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6077302/
https://ncbi.nlm.nih.gov/pubmed/30090038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5217/ir.2018.16.3.393
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