Title:
第１染色体長腕２４領域、ＮＥＵＲＬ遺伝子、またはＣＵＸ２遺伝子の一塩基多型に基づく不整脈の検査方法
Document Type and Number:
Japanese Patent JP5791171
Kind Code:
B2
Abstract:
A method for diagnosing arrhythmia such as atrial fibrillation is provided. A single nucleotide polymorphism present in the region 24 of the long arm of the chromosome 1, NEURL gene, or CUX2 gene is analyzed, and the risk of developing arrhythmia and/or the presence or absence of the onset of arrhythmia is diagnosed on the basis of the analysis result.
Inventors:
Koichi Ozaki
Toshihiro Tanaka
Toshihiro Tanaka
Application Number:
JP2011044157A
Publication Date:
October 07, 2015
Filing Date:
March 01, 2011
Export Citation:
Assignee:
RIKEN
International Classes:
C12N15/09; C12Q1/68
Other References:
Eur. Heart J., (2009), 30, [7], p.813-819
Circulation, (2010), 122, [10], p.976-984
Circ. Arrhythm. Electrophysiol., (2011.02), 4, [1], p.87-93
Cardiovasc. Res., (2005), 67, [3], p.520-528
Circulation, (2010), 122, [10], p.976-984
Circ. Arrhythm. Electrophysiol., (2011.02), 4, [1], p.87-93
Cardiovasc. Res., (2005), 67, [3], p.520-528
Attorney, Agent or Firm:
Yoshiyuki Kawaguchi
Hidemi Matsukura
Shinichi Sanuki
Hidemi Matsukura
Shinichi Sanuki