A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats (Q34184346)

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A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats
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    A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats (English)
    Blue-leaf A Hannah
    Tina M Misenheimer
    Douglas S Annis
    Deane F Mosher
    8929-8934

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