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Volumn 23, Issue 3, 2006, Pages 265-268

Study on novel mutations MEF2A gene in Chinese patients with coronary artery disease

Author keywords

Coronary artery disease; Gene mutation; MEF2A gene

Indexed keywords

PROTEIN MEF2A; TRANSCRIPTION FACTOR IIA; UNCLASSIFIED DRUG;

EID: 33745322160     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (10)
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    • Wang, L.1    Fan, C.2    Topol, S.E.3
  • 2
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    • Transcription factor MEF2A mutations in patients with coronary artery disease
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  • 5
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    • Lack of MEF2A mutations in coronary artery disease
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    • Weng, L.1    Kavaslar, N.2    Ustaszewska, A.3
  • 6
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  • 7
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    • (2005) J Clin Invest , vol.115 , pp. 1399-1400
    • Wang, Q.1    Rao, S.2    Topol, E.J.3
  • 8
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    • Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families
    • Priori SG, Napolitano C, Gasparini M, et al. Clinical and genetic heterogeneity of right bundle branch block and ST-segment elevation syndrome: A prospective evaluation of 52 families. Circulation, 2000, 102:2509-2515.
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  • 9
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.