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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Detalles Bibliográficos
Autores principales: Yamaguchi, Satoko, Yanai, Shunichi, Nakamura, Shotaro, Kawasaki, Keisuke, Eizuka, Makoto, Uesugi, Noriyuki, Sugai, Tamotsu, Umeno, Junji, Esaki, Motohiro, Matsumoto, Takayuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for the Study of Intestinal Diseases 2018
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077302/
https://www.ncbi.nlm.nih.gov/pubmed/30090038
http://dx.doi.org/10.5217/ir.2018.16.3.393

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6077302/
https://www.ncbi.nlm.nih.gov/pubmed/30090038
http://dx.doi.org/10.5217/ir.2018.16.3.393

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