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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Detalhes bibliográficos
Publicado no:Intest Res
Main Authors: Yamaguchi, Satoko, Yanai, Shunichi, Nakamura, Shotaro, Kawasaki, Keisuke, Eizuka, Makoto, Uesugi, Noriyuki, Sugai, Tamotsu, Umeno, Junji, Esaki, Motohiro, Matsumoto, Takayuki
Formato: Artigo
Idioma:Inglês
Publicado em: Korean Association for the Study of Intestinal Diseases 2018
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Original Article
Acesso em linha: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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