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JBC.M211185200
JBC.M211185200
http://dx.doi.org/10.1074/JBC.M211185200
A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats.
P356
Q34184346-33B55EE6-1EB4-4D4C-BDEA-3E63B23F8EA1
P356
JBC.M211185200
http://dx.doi.org/10.1074/JBC.M211185200