Novel 6-bp deletion in MEF2A linked to premature coronary artery disease in a large Chinese family

The aim of the present study was to identify the genetic defect responsible for familial coronary artery disease/myocardial infarction (CAD/MI), which exhibited an autosomal dominant pattern of inheritance, in an extended Chinese Han pedigree containing 34 members. Using exome and Sanger sequencing,...

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Detalles Bibliográficos
Autores principales: XU, DONG-LING, TIAN, HONG-LIANG, CAI, WEI-LI, ZHENG, JIE, GAO, MIN, ZHANG, MING-XIANG, ZHENG, ZHAO-TONG, LU, QING-HUA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918543/
https://www.ncbi.nlm.nih.gov/pubmed/27221044
http://dx.doi.org/10.3892/mmr.2016.5297

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918543/
https://www.ncbi.nlm.nih.gov/pubmed/27221044
http://dx.doi.org/10.3892/mmr.2016.5297

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