Reduced risk of recurrent myocardial infarction in homozygous carriers of the chromosome 9p21 rs1333049 C risk allele in the contemporary percutaneous coronary intervention era: a prospective observational study

OBJECTIVES: Chromosome 9p21 single nucleotide polymorphism (SNP) is a susceptibility variant for acute myocardial infarction (AMI) in the primary prevention setting. However, it is controversial whether this SNP is also associated with recurrent myocardial infarction (ReMI) in the secondary preventi...

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Detalles Bibliográficos
Autores principales: Hara, Masahiko, Sakata, Yasuhiko, Nakatani, Daisaku, Suna, Shinichiro, Usami, Masaya, Matsumoto, Sen, Ozaki, Kouichi, Nishino, Masami, Sato, Hiroshi, Kitamura, Tetsuhisa, Nanto, Shinsuke, Hamasaki, Toshimitsu, Tanaka, Toshihiro, Hori, Masatsugu, Komuro, Issei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2014
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139637/
https://www.ncbi.nlm.nih.gov/pubmed/25232560
http://dx.doi.org/10.1136/bmjopen-2014-005438

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4139637/
https://www.ncbi.nlm.nih.gov/pubmed/25232560
http://dx.doi.org/10.1136/bmjopen-2014-005438

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