Associated Papers
The Involvement of Krüppel-like Factors in Cardiovascular Diseases.
Santoyo-Suarez MG et al.
Life (basel, Switzerland), 2023
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
Identification and analysis of KLF13 variants in patients with congenital heart disease.
Li W et al.
Bmc Medical Genetics, 2020
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