Clinical features of chronic enteropathy associated with SLCO2A1 gene: a new entity clinically distinct from Crohn’s disease

Chronic Enteropathy Associated With SLCO2A1 Gene [CEAS]—Characterisation of an Enteric Disorder to be Considered in the Differential Diagnosis of Crohn’s Disease

(2017) Naoki Hosoe et al.   Journal of Crohns & Colitis

Pediatric-onset Chronic Nonspecific Multiple Ulcers of Small Intestine

(2017) Keiichi Uchida et al.   JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION

Human genetic variation database, a reference database of genetic variations in the Japanese population

(2016) Koichiro Higasa et al.   JOURNAL OF HUMAN GENETICS

A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter

(2015) Junji Umeno et al.   PLoS Genetics

Predicting the Functional Effect of Amino Acid Substitutions and Indels

(2012) Yongwook Choi et al.   PLoS One

Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

(2011) Zhenlin Zhang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Chronic nonspecific multiple ulcer of the small intestine segregates in offspring from consanguinity

(2011) Takayuki Matsumoto et al.   Journal of Crohns & Colitis

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Review: Advances in the diagnosis and treatment of small bowel lesions with Crohn’s disease using double-balloon endoscopy

(2009) Keijiro Sunada et al.   Therapeutic Advances in Gastroenterology

Mutations in 15-hydroxyprostaglandin dehydrogenase cause primary hypertrophic osteoarthropathy

(2008) Sandeep Uppal et al.   NATURE GENETICS