CareLit · DOI-Nachweis · Zeitschrift für Gastroenterologie
Common NOD2/CARD15 alleles and other EXON4 mutations in 527 hungarian patients with Crohn's disease: Genotype-phenotype associations
DOI 10.1055/s-2004-826979
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Nachweis in CareLit
Autor:innenL Lakatos, PL Lakatos, F Szalay, C Willheim-Polli, Z Tulassay, T Molnar, W Reinisch, C Österreicher, J Papp
ZeitschriftZeitschrift für Gastroenterologie
Ausgabe05/2004
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background: Mutations of NOD2/CARD15 gene were identified as genetic markers in Crohn's disease (CD). Our aim was to determine the presence of common NOD2 mutation in 3 cohorts of Hungarian CD patients. Patients and methods: 527 patients with CD (m/f: 265/262, age: 37.1 (SD 7.6)yrs) and 200 healthy subjects were investigated. DNA was screened for possible mutations by denaturing HPLC (WAVE-systems, UK) using publish…
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Zitierempfehlung
L Lakatos, PL Lakatos, F Szalay, C Willheim-Polli, Z Tulassay, T Molnar, W Reinisch, C Österreicher, J Papp (2004) Common NOD2/CARD15 alleles and other EXON4 mutations in 527 hungarian patients with Crohn's disease: Genotype-phenotype associations. Zeitschrift für Gastroenterologie (05). https://doi.org/10.1055/s-2004-826979
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