KLHL26 and Ebstein anomaly: The MYH7 has been identified as the strongest genetic link to bothsporadic and familial cases of this disease, however associations with othergenes such as TPM1, Kelch like family member 26 (KLHL26), FLNA orNKX2-5 are also related to Ebstein’s anomaly, albeit with lesssupporting data [30, 45, 46, 47].