A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter
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Title
A Hereditary Enteropathy Caused by Mutations in the SLCO2A1 Gene, Encoding a Prostaglandin Transporter
Authors
Keywords
Prostaglandin, Anemia, Mutation, Ulcers, Enteropathies, Small intestine, Gastrointestinal tract, Mutation databases
Journal
PLoS Genetics
Volume 11, Issue 11, Pages e1005581
Publisher
Public Library of Science (PLoS)
Online
2015-11-06
DOI
10.1371/journal.pgen.1005581
References
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Note: Only part of the references are listed.- Association Study of 71 European Crohnʼs Disease Susceptibility Loci in a Japanese Population
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- Chronic nonspecific multiple ulcer of the small intestine segregates in offspring from consanguinity
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- A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population
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