Loss of function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype

Maruthappu, T; Posafalvi, A; Castelletti, S; Delaney, PJ; Syrris, P; O'Toole, EA; Green, KJ; ... Kelsell, DP; + view all Maruthappu, T; Posafalvi, A; Castelletti, S; Delaney, PJ; Syrris, P; O'Toole, EA; Green, KJ; Elliott, PM; Lambiase, PD; Tinker, A; McKenna, WJ; Kelsell, DP; - view fewer (2018) Loss of function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype. British Journal of Dermatology 10.1111/bjd.17388 . (In press).

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