CareLit · DOI-Nachweis · Aktuelle Neurologie
Sequence variation in the gene encoding soluble epoxide hydrolase (EPHX2) is associated with increased susceptibility to ischemic stroke in a central european population
DOI 10.1055/s-2007-987777
Bibliografische Angaben
Nachweis in CareLit
Autor:innenA Gschwendtner, S Ripke, T Freilinger, B Müller-Myhsok, T Meitinger, M Dichgans
ZeitschriftAktuelle Neurologie
Ausgabe09/2007
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Background and purpose: Recent evidence suggests that genetic variation in the EPHX2 gene region modifies individual risk of ischemic stroke. The role of EPHX2 has not yet been explored with regard to stroke subtypes, however. Our goal was to replicate the original findings in a large and well-characterized sample of central European patients; additionally, we set out to examine the role of EPHX2 with regard to spec…
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Zitierempfehlung
A Gschwendtner, S Ripke, T Freilinger, B Müller-Myhsok, T Meitinger, M Dichgans (2007) Sequence variation in the gene encoding soluble epoxide hydrolase (EPHX2) is associated with increased susceptibility to ischemic stroke in a central european population. Aktuelle Neurologie (09). https://doi.org/10.1055/s-2007-987777
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