Interleukin-17A gene polymorphism with the susceptibility of intestinal symptoms in patients with Behçet's disease
J Dermatol
.
2016 Jun;43(6):708-9.
doi: 10.1111/1346-8138.13251.
Epub 2016 Jan 30.
Authors
Koichiro Nakamura
1
2
,
Kyohei Miyano
1
2
,
Tetsuya Tsuchida
1
,
Akira Meguro
3
,
Nobuhisa Mizuki
3
Affiliations
1
Department of Dermatology, Saitama Medical University, Saitama, Japan.
2
Allergy Center, Saitama Medical University, Iruma- gun, Saitama, Japan.
3
Department of Ophthalmology, Yokohama City University, Yokohama, Japan.
PMID:
26826002
DOI:
10.1111/1346-8138.13251
No abstract available
Publication types
Letter
MeSH terms
Behcet Syndrome / genetics*
Case-Control Studies
Humans
Interleukin-17 / genetics*
Intestinal Diseases / genetics*
Polymorphism, Single Nucleotide
Substances
IL17A protein, human
Interleukin-17