GeneticsEuropean Heart JournalPeer-reviewed
A rare missense mutation in MYH6 confers high risk of coarctation of the aorta
Þorsteinn Björnsson, Rósa B. Þórólfsdóttir, Garðar Sveinbjörnsson…·Kāri Stefánsson
The paper identifies a rare missense mutation in MYH6 associated with increased risk of coarctation of the aorta and other cardiac conditions.
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