Lack of MEF2A Δ7aa mutation in Irish families with early onset ischaemic heart disease, a family based study

BACKGROUND: Ischaemic heart disease (IHD) is a complex disease due to the combination of environmental and genetic factors. Mutations in the MEF2A gene have recently been reported in patients with IHD. In particular, a 21 base pair deletion (Δ7aa) in the MEF2A gene was identified in a family with an...

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Detalhes bibliográficos
Main Authors: Horan, Paul G, Allen, Adrian R, Hughes, Anne E, Patterson, Chris C, Spence, Mark, McGlinchey, Paul G, Belton, Christine, Jardine, Tracy CL, McKeown, Pascal P
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2006
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1552052/
https://ncbi.nlm.nih.gov/pubmed/16872533
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-7-65
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