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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...
| Autores principales: | , , , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2006
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1552052/ https://www.ncbi.nlm.nih.gov/pubmed/16872533 http://dx.doi.org/10.1186/1471-2350-7-65 |