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The aim of this study was to describe the MEF2A gene in individuals had early-onset ischaemic heart disease
Abstract:
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 (Delta7aa) in the MEF2A gene was identified in a family with an autosomal dominant pattern of inheritance of IHD. We investigated this region of the more...
International Classification:
Diseases of the circulatory system - ischaemic heart disease
Categories:
ischaemic heart disease
Geography:
Northern Ireland
BMC Med Genet,
Vol: 7 Page: 65 2006
P. G. Horan; A. R. Allen; A. E. Hughes; C. C. Patterson; M. Spence; P. G. McGlinchey; C. Belton; T. C. Jardine; P. P. McKeown
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