The University of Chicago Header Logo

Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction.

Novel KLHL26 variant associated with a familial case of Ebstein's anomaly and left ventricular noncompaction. Mol Genet Genomic Med. 2020 04; 8(4):e1152.

View in: PubMed