Associated Papers
KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.
Guo YH et al.
Journal of the American Heart Association, 2022
A novel KLF13 mutation underlying congenital patent ductus arteriosus and ventricular septal defect, as well as bicuspid aortic valve.
Abhinav P et al.
Experimental and Therapeutic Medicine, 2022
KLF13 loss-of-function variation contributes to familial congenital heart defects.
Wang SS et al.
European Review for Medical and Pharmacological Sciences, 2020
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