Illuminating Kir channel function in Anderson –Tawil syndrome

This editorial refers to ‘Impaired cytoplasmic domain interactions cause co-assembly defect and loss of function in the p.Glu293Lys KNCJ2 variant isolated from an Andersen–Tawil syndrome patient’, by S. Dériet al., pp. 1923 –1934.
Source: Cardiovascular Research - Category: Cardiology Source Type: research