Prevalence of SLC22A4, SLC22A5 and CARD15 gene mutations in Hungarian pediatric patients with Crohn’s disease

AIM: 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). METHODS: A cohort of 19 unrelated pediatric and 55 unrelated adult patients with Crohn’s di...

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Detaylı Bibliyografya
Asıl Yazarlar: Bene, Judit, Magyari, Lili, Talián, Gábor, Komlósi, Katalin, Gasztonyi, Beáta, Tari, Beáta, Várkonyi, Ágnes, Mózsik, Gyula, Melegh, Béla
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Baishideng Publishing Group Co., Limited 2006
Konular:
Rapid Communication
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4088243/
https://ncbi.nlm.nih.gov/pubmed/17006998
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v12.i34.5550
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