Open AccessPrevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn’s disease
Author(s) -
Judit Bene,
Lili Magyari,
Gábor Talián,
Katalin Komlósi,
Beáta Gasztonyi,
B Tari,
Á. Várkonyi,
Gyula Mózsik,
Béla Melegh
Publication year - 2006
Publication title -
world journal of gastroenterology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.427
H-Index - 155
eISSN - 2219-2840
pISSN - 1007-9327
DOI - 10.3748/wjg.v12.i34.5550
Subject(s) - genotyping , crohn's disease , medicine , allele frequency , cohort , inflammatory bowel disease , gastroenterology , allele , genotype , immunology , disease , genetics , biology , gene
To investigate the frequency of the common NOD2/CARD15 susceptibility variants and two functional polymorphisms of OCTN cation transporter genes in Hungarian pediatric patients with Crohn's disease (CD).