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

ACG Clinical Guideline: Diagnosis and Management of Small Bowel Bleeding

(2015) Lauren B Gerson et al.   AMERICAN JOURNAL OF GASTROENTEROLOGY

Clinical Characteristics and Treatment Outcomes of Cryptogenic Multifocal Ulcerous Stenosing Enteritis in Korea

(2015) Sook Hee Chung et al.   DIGESTIVE DISEASES AND SCIENCES

Small-bowel capsule endoscopy and device-assisted enteroscopy for diagnosis and treatment of small-bowel disorders: European Society of Gastrointestinal Endoscopy (ESGE) Clinical Guideline

(2015) Marco Pennazio et al.   ENDOSCOPY

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

(2015) Junji Umeno et al.   PLoS Genetics

The complete type of pachydermoperiostosis: A novel nonsense mutation p.E141* of the SLCO2A1 gene

(2014) H. Niizeki et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Mutations in theSLCO2A1Gene and Primary Hypertrophic Osteoarthropathy: A Clinical and Biochemical Characterization

(2013) Zeng Zhang et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α

(2012) Matthew A Brooke et al.   GUT

Prostaglandin transporter mutations cause pachydermoperiostosis with myelofibrosis

(2012) Christine P. Diggle et al.   HUMAN MUTATION

Mutations in the Prostaglandin Transporter SLCO2A1 Cause Primary Hypertrophic Osteoarthropathy with Digital Clubbing

(2012) Jutta Busch et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

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